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Paracetamol Suppositories Rect., Packaging No Less Than 250 Mg No. 6. Composition Of The Medicinal Product. One Suppository Contains Active Substance - Paracetamol 125 Mg Or 250 Mg, Excipient: Solid Fat. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Solution For Injection Not Less Than 0.5% -5 Ml No. 10. Composition Of The Medicinal Product 1 Ml Of Solution Contains Active Substance - Procaine Hydrochloride 5.0 Mg 20.0 Mg Excipients: Solution Of 0.1 M Hydrochloric Acid, Water For Injection Description Of Appearance, Smell, Taste Transparent, Colorless Or Slightly Colored Solution., Ointment At Least 10% 20 Gr. Composition Of The Medicinal Product 20 G Ointment Contains Active Substance - Povidone-Iodine 2 G (Equivalent To Active Iodine 200 Mg), Excipients: Sodium Bicarbonate, Macrogol 400, Macrogol 1000, Macrogol 1500, Macrogol 4000, Purified Water. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Drops Of At Least 50 Ml. Bottle, Composition Of The Medicinal Product: 10 G (=9.75 Ml) Solution Contains Active Substance - Pelargonium Sidoides Roots Extract Liquid (1:8 – 10) (Extractant: Ethanol 11%) - 8.0 G; Excipient – Glycerin 85% Description Of Appearance, Smell, Taste The Liquid Is Light Brown To Reddish Brown. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Drops For Oral Administration, Bottle Packaging Of At Least 100 Ml. Pharmacotherapeutic Group Genitourinary System And Sex Hormones. Urological Drugs. Urological Drugs Are Different. Composition Of The Medicinal Product 100 G Of The Drug Contains Active Substance: 29 G Of Aqueous-Alcoholic Extract From The Medicinal Vegetable Raw Materials: Centaury Grass 0.6 G Lovage Medicinal Roots 0.6 G Rosemary Leaves 0.6 G Excipients: Ethanol 59%, Purified Water. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Solution For Inhalation, Bottle Of At Least 20 Ml. Pharmacotherapeutic Group. Respiratory System. Drugs For The Treatment Of Obstructive Airway Diseases. Adrenergic, Inhalation. Adrenergic Drugs In Combination With Anticholinergics, Including Triple Combinations With Corticosteroids. Fenoterol And Ipratropium Bromide. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Suppositories Rect. Packaging Of At Least 150,000 Iu No. 10 Candles. Composition Of The Medicinal Product One Suppository Contains Active Substance - Interferon Alpha-2B Human Recombinant 150,000 Iu, Excipients: Ascorbic Acid, Sodium Ascorbate, Alpha-Tocopherol Acetate, Disodium Edetate Dihydrate, Polysorbate-80, Cocoa Butter, Confectionery Fat Or Cocoa Butter Substitute. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Non-Sterile Cotton Wool, At Least 50 G. Made From 100% First Grade Cotton Fiber., Water For Injection, At Least 5 Ml No. 10. Composition 1 Ml Contains Active Substance – Water For Injection 1.0 Ml., A Container For Collecting Excrement Of At Least 60 Ml With A Screw-On Lid, Container For Collecting Biomaterials, At Least 125 Ml, Sterile, Butterfly Needle Size No Less Than 21 G*3.4, Elastic Medical Bandage Of High Extensibility, At Least 10 Cm X 5 M, Disposable Syringe, At Least 50 G, Solution For Injection, Packaging Of At Least 1 Ml No. 5. Composition 1 Ml Of Solution Contains Active Substance - Chloropyramine Hydrochloride 20 Mg, Excipient - Water For Injection. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Lyophilisate For The Preparation Of Solution For Injection And Inhalation, Complete With Solvent, Packaging Of At Least 500 Mg No. 3. Composition Of The Medicinal Product One Bottle Contains Active Substance - Thiamphenicol Glycinate Acetylcysteinate 810 Mg (Equivalent To Thiamphenicol 500 Mg), Excipient – Disodium Edetate. Solvent – Water For Injection. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Injection Solution Of At Least 0.18% 1 Ml No. 10 In Amp. Active Substance: Epiphrine; 1 Ml Of Solution Contains Adrenaline Hydrotratrate (Adrenaline Tartrate) 1.8 Mg; Excipients: Sodium Metabisulfite (E 223), Sodium Chloride, Water For Injection. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Hypoallergenic Adhesive Plaster No Less Than 2.5Cm X 5M, Suspension For Oral Use, Packaging Not Less Than 2.4% 100 Ml. Composition 100 Ml Of Suspension Contain Active Substance – Paracetamol 2.4 G, Excipients - Sorbitol, Distilled Glycyrin, Carbomer, Methylparaben, Propylparaben, Citric Acid, Sodium Citrate, Sodium Saccharinate, Food Flavoring, Red Sour Dye 2C, Purified Water The Drug Does Not Contain Alcohol. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Diamond Green Alcohol Solution At Least 1% 30 Ml. Composition Of The Medicinal Product 100 Ml Of The Drug Contains Active Ingredients: Brilliant Green - 1 G Excipient: Ethyl Alcohol 60%, Syrup, Packaging Of At Least 250 Mg/5 Ml, 150 Ml. Composition Of The Medicinal Product 1 Ml Of Syrup Contains Active Substance - Inosine Pranobex 50.00 Mg Excipients: Methyl Parahydroxybenzoate, Propyl Parahydroxybenzoate, Sucrose, Sodium Hydroxide, Citric Acid Monohydrate, Purified Water. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Ointment For External Use, Packaging Not Less Than 05% 30. Composition Of The Medicinal Product 1 G Ointment Contains: Active Substance: Betamethasone Dipropionate, 0.640 Mg (Equivalent To 0.500 Mg Betamethasone); Excipients: Petroleum Jelly, Petroleum Jelly. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Solution, Bottle Packaging Of At Least 7.5 Mg/Ml, 100 Ml. 1 Ml Of The Drug Contains Active Substance - Ambroxol Hydrochloride 7.5 Mg, Excipients – Potassium Sorbate, Hydrochloric Acid 25% (For Ph Correction), Purified Water. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Tablets Packaging Of At Least 25 Mg No. 100. Composition Of The Medicinal Product One Tablet Contains Active Substance – Levothyroxine Sodium 0.025 Mg, 0.050 Mg, 0.075 Mg, 0.100 Mg, 0.125 Mg And 0.150 Mg, Excipients: Mannitol, Corn Starch, Gelatin, Croscarmellose Sodium, Anhydrous Citric Acid, Magnesium Stearate. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Suspension For Oral Administration, Packaging Of At Least 3 G No. 12. Composition Of The Medicinal Product One Sachet Contains Active Substance – Dioctahedral Smectite (Diosmectite), 3 G Excipients: Caramel-Cocoa Flavor*, Xanthan Gum, Hydrochloric Acid, Sodium Benzoate, Potassium Sorbate, Sucralose, Purified Water. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Syrup, Packaging Not Less Than 250 Mg/5 Ml. 150Ml. Composition Of The Medicinal Product 1 Ml Syrup Contains Active Substance - Inosine Pranobex, 50 Mg Excipients: Sucrose, Methyl Parahydroxybenzoate (E 218), Propyl Parahydroxybenzoate (E 216), Citric Acid Monohydrate, Sodium Citrate, Flavoring, Purified Water. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Cream At Least 2% 15 G. Composition Of The Medicinal Product 1 G Of Cream Contains Active Substance - Ketoconazole 20 Mg, Excipients: Propylene Glycol, Cetostearyl Alcohol, Cetomacrogol 1000, White Soft Paraffin, Light Liquid Paraffin, Disodium Edetate, Polysorbate 80, Anhydrous Sodium Sulfite, Purified Water. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Oil At Least 50 Ml. Composition Of The Medicinal Product 100 G Of The Drug Contains Active Ingredients: Lemon Balm Herb 0.20 G, Creeping Thyme Herb 0.20 G, Rosehip Fruits 1.0 G, Licorice Roots 1.60 G, Nettle Leaves 2.0 G, St. Johns Wort Herb 12.0 G, Sea Buckthorn Oil 1.60 G Excipient: Sunflower Oil. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Powder At Least 3 G No. 10. Composition Lyophilized Lactic Acid Bacteria Lactobacillus Rhamnosusgg, Maltodextrin - 2155 Mg, Fructooligosaccharides - 800 Mg, Silicon Dioxide (E 551) - 5 Mg. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Gel For External Use At Least 2% 40 Gram Gel. Composition Of The Medicinal Product 100 G Of Gel Contains: Active Substance – Troxerutin 2G, Excipients - Carbomer, Disodium Edta, Benzalkonium Chloride, Triethanolamine, Purified Water. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Paste For Oral Administration, Packaging Not Less Than 225 G. Composition 100 G Contain: Active Substance - Polymethylsiloxane Polyhydrate (Nonlinear Polycondensation Product 1, 1, 3, 3 - Tetrahydroxy-1,3-Dimethyldisiloxane Polyhydrate) 70 G. Excipient - Purified Water 30 G. The Product And Shelf Life Must Comply With All Norms And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicinal Products And Medical Devices., Gel Packaging Of At Least 0.1% - 30G For External Use. Composition Of The Medicinal Product 1 G Of The Drug Contains: Active Substance – Dimethindene Maleate 1 Mg, Excipients: Propylene Glycol, 30% Sodium Hydroxide Solution, Carbomer, Disodium Edetate, 50% Benzalkonium Chloride Solution, Purified Water. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Syrup, At Least 150 Ml. Composition Of The Medicinal Product 5 Ml Syrup Contains Active Substances: Retinol Palmitate 1.7 Million Iu/G (Vitamin A) 900 Iu Cholecalciferol 1 Million Iu/G (Vitamin D3) 100 Iu Ascorbic Acid (Vitamin C) 50,000 Mg Thiamine Hydrochloride (Vitamin B1) 1,000 Mg Riboflavin Sodium Phosphate (Vitamin B2) 1,000 Mg Pyridoxine Hydrochloride (Vitamin B6) 0.600 Mg Cyanocobalamin (Vitamin B12) 0.001 Mg Nicotinamide (Vitamin Pp) 5,000 Mg Dexpanthenol (D – Panthenol) 2,000 Mg Excipients: Agar, Tragacanth, Sucrose, Liquid Glucose, Orange Flavor Oil, Grapefruit Flavor, Orange Flavor, Polysorbate 80, Citric Acid Monohydrate, Ponceau 4R Dye (E124), Sodium Benzoate, Purified Water. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Solution For External Use, Not Less Than 100 Ml. Composition Of The Medicinal Product 100 Ml Of The Drug Contains: Active Substance - Hydrogen Peroxide Solution (Hydrogen Peroxide Content In The Original Substance From 27% To 40%) - From 7.5 To 11.11 G (Depending On The Actual Content Of Hydrogen Peroxide In The Original Substance); Excipient – Sodium Benzoate, Purified Water., Eye Ointment, Packaging Not Less Than 3% 5G. Composition Of The Medicinal Product 1 G Ointment Contains Active Substance - Acyclovir 0.03 G, Excipient: White Soft Paraffin (Vaseline) Up To 1.00 G. The Product And Shelf Life Must Comply With All Norms And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicinal Products And Medical Devices., Drops Of At Least 50 Ml. Composition Active Ingredients: Carduus D1 - 2 Ml, Taraxacum D6 - 10 Ml, Chelidonium D6 - 10 Ml, Natrium Sulfuricum D12 - 10 Ml, Phosphorus D12 - 10 Ml; Excipient: Ethanol 43% By Weight., Chewable Tablets Packaging No Less Than No. 120. Composition Of The Medicinal Product One Tablet Contains Active Ingredients: Calcium Carbonate 1250 Mg (Equivalent To Elemental Calcium 500 Mg), Cholecalciferol 5.5 Mcg (200 Iu Vitamin D3) In The Form Of Cholecalciferol Concentrate* 2.20 Mg, *Cholecalciferol Concentrate Contains, Including 10% Excess: Cholecalciferol 0.00550 Mg, Dl-Α-Tocopherol 0.0220 Mg, Medium Chain Triglycerides 0.0660 Mg, Modified Corn Starch 1.61 Mg, Sucrose 0.385 Mg, Sodium Ascorbate 0.0880 Mg, Silicon Dioxide 0.0264 Mg. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Solution For Injection Not Less Than 2% 20 Mg/Ml, 2 Ml. No. 10. Composition Of The Medicinal Product One Ampoule (2 Ml) Contains: Active Substance - Papaverine Hydrochloride 40 Mg; Excipients: Disodium Edetate, Dl-Methionine, Water For Injection., Film-Coated Tablets Of At Least 50 Mg No. 30. Composition One Tablet Contains Active Substance - Tolperisone Hydrochloride 50 Mg And 150 Mg, Excipients: Anhydrous Citric Acid, Colloidal Silicon Dioxide, Stearic Acid, Talc, Microcrystalline Cellulose, Corn Starch, Lactose Monohydrate, Film Shell Composition: Anhydrous Colloidal Silicon Dioxide, Titanium Dioxide (E 171), Lactose Monohydrate, Macrogol 6000, Hypromellose. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Iodine Solution At Least 5% - 20 Ml Solution. Composition Of The Medicinal Product 100 Ml Of The Drug Contains Active Substances – Iodine 5.0 G, Potassium Iodide 2.0 G Excipient – Ethyl Alcohol 50%., Nasal Spray Not Less Than 125 Ml. Content Composition Natural Sea Water, Purified Water Ph 6.0 - 8.5 Nacl Content 8 - 11 G/L. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Ear Drops Not Less Than 10 Ml. Composition: Allantoin 3 Mg Benzetoin Chloride 1 Mg Butylated Hydroxytoulene 1 Mg Phenethanol 5 Mg Sorbic Acid 2 Mg Liquid Lanolin Mink Oil Fillers And Emulsifiers Purified Water Up To 1 Ml. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Tablets, At Least 200 Mg. No. 50. Composition Of The Medicinal Product One Tablet Contains Active Substance – Hymecromone 200 Mg Excipients: Potato Starch, Gelatin, Sodium Lauryl Sulfate, Magnesium Stearate. Description Of Appearance, Smell, Taste Tablets Are Round In Shape, With A Flat Surface, White Or White With A Yellowish Tint, Engraved On One Side With The Letters “Ch”, With A Diameter Of 8.8 To 9.3 Mm., Drops For Oral Administration Of At Least 10 Ml. Composition Of The Medicinal Product One Ml Of The Drug Contains Active Substance - Colecalciferol, 15,000 Iu, Excipients: Macrogol Glyceryl Ricinoleate, Sucrose, Disodium Phosphate Dodecahydrate, Citric Acid Monohydrate, Anise Flavor, Benzyl Alcohol, Purified Water. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Spatula No. 100, Nasal Drops Not Less Than 0.05% 10Ml. Composition 1 Ml Of Solution Contains Active Substance - Oxymetazoline Hydrochloride 0.1 Mg, 0.25 Mg And 0.5 Mg, Excipients: Citric Acid Monohydrate, Sodium Citrate Dihydrate, Glycerol (85%), Benzalkonium Chloride (50% Solution), Purified Water. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Solution For Injection, Not Less Than 25%, 5 Ml No. 5. Composition Of The Medicinal Product 5 Ml Of The Drug Contain Active Substance – Magnesium Sulfate Heptahydrate 1.25 G, Excipient – Water For Injection., Film-Coated Tablets Of At Least 10 Mg, No. 60. Composition Of The Medicinal Product One 10 Mg Film-Coated Tablet Contains: Active Substance - Thioridazine Hydrochloride 10.0 Mg, Excipients: Corn Starch, Colloidal Silicon Dioxide, Lactose, Gelatin, Stearic Acid, Talc. Shell Composition: Sucrose, Gum Arabic, Talc, Red Cochineal A (E124)., Drops Of At Least 5 Ml. Composition Of The Medicinal Product One Ml Of Solution Contains Active Substances: Dexamethasone (As Dexamethasone Sodium Phosphate) 1 Mg, Neomycin (As Neomycin Sulfate) 5 Mg, Excipients: Disodium Phosphate Dodecahydrate, Water For Injection. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Aerosol For External Use, Packaging Not Less Than 116 G. Composition Of The Medicinal Product 100 G Of The Drug Contains Active Substance - Dexpanthenol 4.310 G Excipients: Cetostearyl Emulsifying Alcohol (Type A), Methyl Parahydroxybenzoate, Macrogolglycerol Cocoate, Propylene Glycol, Potassium Dihydrogen Phosphate, Disodium Phosphate Dodecahydrate, Purified Water, Freon 134A. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Suspension For Oral Use, Packaging Of At Least 4 Billion/5 Ml No. 10. Composition Of The Medicinal Product 5 Ml Bottle Contains Active Substance - Bacillus Clausii Spores, Multiresistant To Antibiotics 4 Billion, Excipient - Purified Water. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Suspension, Packaging Not Less Than 220 Mg/5 Ml, 90 Ml. Composition Of The Medicinal Product 5 Ml Of The Drug Contain Active Substance - Nifuroxazide 220 Mg, Excipients: Citric Acid, Sodium Hydroxide, Banana Essence, Methyl Parahydroxybenzoate, Carbomer, Simethicone Emulsion 30%, Sucrose, Purified Water. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Tablets, Packaging Of At Least 10 Mg. No. 10. Composition One Tablet Contains Active Substance - Loratadine 10.00 Mg, Excipients: Lactose Monohydrate, Corn Starch, Magnesium Stearate. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Spray At Least 1% 30 Ml. For Local Use. Composition Of The Medicinal Product One Bottle Contains Active Substance - Terbinafine Hydrochloride 0.3 G, Excipients: Ethanol 96%, Macrogol (Eumulgin B2), Propylene Glycol (Monopropylene Glycol), Purified Water. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Tablets, Packaging Of At Least 30 Mg No. 20. Composition Of The Medicinal Product. One Tablet Contains Active Substance – Ambroxol Hydrochloride 30.0 Mg, Excipients: Lactose Monohydrate, Microcrystalline Cellulose, Pregelatinized Starch, Colloidal Anhydrous Silicon Dioxide (Aerosil), Calcium Stearate. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Cream At Least 50 Gr. Composition 1 G Of Cream Contains Active Ingredients: Dexpanthenol – 52.5 Mg, Chlorhexidine Bigluconate 20% Solution – 42.7 Mg, (Equivalent To Chlorhexidine Bigluconate – 8.02 Mg), Excipients: Propylene Glycol, Macrogol Cetostearate, Cetostearyl Alcohol (Cetyl Alcohol No More Than 60%, Stearyl Alcohol No Less Than 40%), Liquid Paraffin, Petroleum Jelly, Sodium Hydrogen Phosphate Dodecahydrate, Potassium Dihydrogen Phosphate, Purified Water. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Ointment For External Use, At Least 30G. Tuba Composition Of The Medicinal Product 1 G Of The Drug Contains Active Ingredients: Betamethasone Dipropionate 0.640 Mg (Equivalent To 0.500 Mg Betamethasone), Gentamicin Sulfate 1.660 Mg (Equivalent To 1.000 Mg Gentamicin Base); Excipients: Petroleum Jelly, Petroleum Jelly. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Eye Drops, Packaging Not Less Than 0.25% -10Ml. Composition Of The Medicinal Product 1 Ml Of The Drug Contains: Active Substance - Chloramphenicol – 2.5 Mg Excipients – Boric Acid, Water For Injection. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Solution For Intravenous And Intramuscular Administration, Packaging Of At Least 30 Mg/Ml. Composition Of The Medicinal Product 1 Ml Of Solution Contains Active Substance – Prednisolone Sodium Phosphate, Equivalent To Prednisolone Phosphate, 30 Mg Excipients: Disodium Edetate, Disodium Hydrogen Phosphate Anhydrous, Sodium Dihydrogen Phosphate Dihydrate, Propylene Glycol, Phosphoric Acid, Water For Injection. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Drops Of At Least 30 Ml. Remaining Medicinal Product 100 Ml Of Solution Contains Active Substances: Aqueous Substrate Of Metabolic Products Escherichia Coli Dsm 4087 24.9481 G Enterococcus Faecalis Dsm 4086 12.4741 G Lactobacillus Acidophilus Dsm 4149 12.4741 G Lactobacillus Helveticus Dsm 4183 49.8960 G Excipients: Sodium Phosphate Heptahydrate, Potassium Hydrogen Phosphate, Lactic Acid, Concentrated Phosphoric Acid, Potassium Sorbate, Citric Acid Monohydrate. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Capsules Containing Minimicrospheres Coated With An Enteric Coating, Not Less Than 10,000 Capsules 150 Mg No. 20. Composition Of The Medicinal Product One Capsule Contains Active Substance - Pancreatin 150 Mg, With Minimal Enzymatic Activity: Amylase - 8000 Euro Units. F., Lipases - 10000 Eur Units. F., Proteases - 600 Eur Units. F., Excipients Pellet Core: Macrogol 4000, Pellet Shell: Cetyl Alcohol, Hypromellose Phthalate, Triethyl Citrate, Dimethicone 1000, Capsule Shell: Gelatin, Anhydrous Iron (Iii) Oxide (E 172), Hydrated Iron (Iii) Oxide (E 172), Iron (Ii, Iii) Oxide (E 172), Titanium Dioxide (E 171), Sodium Lauryl Sulfate., Ointment Not Less Than 0.1% 15 G. Composition 100 G Ointment Contains Active Substance – Methylprednisolone Aceponate 0.1 G, Excipients: White Beeswax, Liquid Paraffin, Dehymuls E, Soft White Paraffin, Purified Water. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Balsamic Liniment (According To Vishnevsky) Packaging Of At Least 40G. Composition Of The Medicinal Product One Tube (40 G) Contains Active Ingredients: Birch Tar – 1.2 G, Xeroform -1.2 G In Terms Of Bismuth Oxide 0.599 G Excipients: Anhydrous Colloidal Silicon Dioxide, Castor Oil. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Capsules, Packaging Of At Least 60 Mg No. 7. Composition Of The Medicinal Product One Capsule Contains Active Substance – Pentanedioic Acid Imidazolylethanamide (Vitaglutam) Calculated As 100% Substance, 60.0 Mg, Excipients – Lactose Monohydrate, Potato Starch, Colloidal Silicon Dioxide (Aerosil), Magnesium Stearate, Composition Of The Capsule Shell – Titanium Dioxide E171, Iron Dye Yellow Oxide E 172, Gelatin, The Ink Composition For The Logo Is Shellac, Propylene Glycol E1520, Titanium Dioxide E171. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Tablets Not Less Than 20 Mg No. 10. Composition One Tablet Contains Active Substance – Furatsilina 0.02 G Excipient – Sodium Chloride, Cream At Least 2% 40G. Composition Of The Medicinal Product One Gram Of The Drug Contains Active Substance – Silver Sulfathiazole 20.0 Mg Excipients: Cetostearyl Alcohol, Liquid Paraffin, White Petrolatum, Sodium Lauryl Sulfate, Glycerin, Methyl Parahydroxybenzoate, Propyl Parahydroxybenzoate, Potassium Dihydrogen Phosphate, Sodium Hydrogen Phosphate, Water For Injection. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Tablets Of At Least 2.5 Mg No. 20. One Tablet Contains Active Substance – Enalapril Maleate 2.5 Mg, Excipients: Sodium Bicarbonate, Lactose Monohydrate, Corn Starch, Hydroxypropylcellulose, Talc, Magnesium Stearate., Tablets Not Less Than 120 Mg No. 112 Table. Composition Of The Medicinal Product One Tablet Contains Active Substance - Bismuth Tripotassium Dicitrate 303.03 Mg (Equivalent To Bismuth Oxide 120 Mg), Excipients: Corn Starch, Povidone K-30, Potassium Polyacryline, Macrogol 6000, Magnesium Stearate, Shell: Opadry Ii Clear (Composition: Polyvinyl Alcohol, Macrogol 4000, Talc), Titanium Dioxide (E171), Solution For External Use, At Least 10% 20Ml. Composition Of The Medicinal Product 100 Ml Of The Drug Contains Active Substance – Ammonia Concentrated Solution 44.0 Ml Excipient - Purified Water Up To 100.0 Ml Description Of Appearance, Smell, Taste Transparent, Colorless, Very Alkaline Liquid With A Pungent Odor., Ear Drops No Less Than 25 Ml. Composition Of The Medicinal Product 100 Ml Of Solution Contains Active Ingredients: Polymyxin B Sulfate – 1,000,000 Iu, Neomycin Sulfate – 375000 Iu, Lidocaine Hydrochloride – 4.0 G, Excipients: Glycerin, Propylene Glycol, Benzalkonium Chloride, Purified Water. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Tube No. 4 With A Small Diameter For The Device Bop-01/27 (Bop 4), Drops Of At Least 100 Mg/Ml 30 Ml. Composition Of The Medicinal Product 1 Ml (About 20 Drops) Contains Active Substance – Ascorbic Acid 100 Mg Excipients: Anhydrous Glycerin, Purified Water. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Film-Coated Tablets Of At Least 25 Mg, No. 60. Composition Of The Medicinal Product One 25 Mg Film-Coated Tablet Contains: Active Substance - Thioridazine Hydrochloride 25.0 Mg, Excipients: Potato Starch, Sucrose, Gelatin, Magnesium Stearate, Talc Shell Composition: Sucrose, Gum Arabic, Talc, Quinoline Yellow (E110)., Cream At Least 1% 15G. Composition Of The Medicinal Product 1 G Of Cream Contains Active Substance - Terbinafine Hydrochloride 10,000 Mg (Equivalent To Terbinafine 8.888 Mg), Excipients: Sodium Hydroxide, Benzyl Alcohol, Sorbitan Stearate, Cetyl Palmitate, Cetyl Alcohol, Stearyl Alcohol, Polysorbate 60, Isopropyl Myristate, Purified Water. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Syrup, Packaging Of At Least 200 Ml. One Bottle Contains Active Substance – Liquid Lactulose 667 G/L. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Drops, Packaging Not Less Than 10 Mg/Ml 20 Ml. Composition Of The Medicinal Product 1 Ml Of The Drug Contains Active Substance - Cetirizine Dihydrochloride 10 Mg Excipients: Methyl Parahydroxybenzoate, Propyl Parahydroxybenzoate, Glycerin 85%, Propylene Glycol, Sodium Saccharin, Sodium Acetate, Glacial Acetic Acid, Purified Water. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Suspension For Oral Administration, Packaging Of At Least 200 Mg/5 Ml., 100 Ml. Composition Of The Medicinal Product 5 Ml Of Suspension Contain Active Substance - Ibuprofen 200 Mg, Excipients: Hypromellose, Xanthan Gum, Glycerin, Sodium Benzoate, Liquid Maltitol, Sodium Citrate, Citric Acid Monohydrate, Sodium Saccharinate, Sodium Chloride, Strawberry Flavor: Flavoring Agents, Propylene Glycol (E1520), Water; Purified Water. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices, Film-Coated Tablets, Packaging Of At Least 200 Mg No. 10. One Tablet Contains Active Substance – Ibuprofen 200 Mg Excipients: Potato Starch, Magnesium Stearate, Calcium Stearate, Povidone, Opadry Ιι (Contains Polyvinyl Alcohol, Partially Hydrolyzed, Talc, Macrogol 3350, Lecithin, Titanium Dioxide (E 171)). The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices, Drops For Oral Administration Of At Least 25 Ml. Composition Of The Medicinal Product 25 Ml Of Solution Contain Active Substance - Iron (Ii) 0.2370 G (As Sulfate Heptahydrate (1.1800 G)) Excipients: Sorbitol, Ascorbic Acid, Food Flavoring, Purified Water. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Solution Of At Least 20% -120 Ml. Composition Of The Medicinal Product 100 Ml Of The Drug Contains Active Substance - Artichoke (Leaf Extract Thick, Aqueous) 20.0 G, Excipients: Ethyl Alcohol 96%, Glycerin, Methyl Parahydroxybenzoate (E218), Propyl Parahydroxybenzoate (E216), Orange Peel Alcoholate (Flavor), Purified Water., Solution For Injection Not Less Than 500 Mcg/Ml. Composition Of The Medicinal Product One Ampoule (1 Ml) Contains Active Substance – Cyanocobalamin 500 Mcg Excipients: Sodium Chloride, Water For Injection. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Cream For External Use, Packaging No Less Than 5% 5G Ointment For External Use Approx. Composition Of The Medicinal Product 1 G Of Cream Contains Active Substance - Acyclovir 50 Mg, Excipients: Propylene Glycol, Glyceryl Stearate, Polyethylene Glycol-100 Stearate, Cetostearyl Alcohol, White Soft Paraffin, Liquid Paraffin, Sodium Lauryl Sulfate, Purified Water. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Enteric Capsules, No Less Than 20 Mg No. 30. Each Capsule Contains: Active Substance: Omeprazole – 20 Mg (In Pellet Form 8.5%); Excipients: Mannitol, Disodium Hydrogen Phosphate, Calcium Carbonate, Sodium Lauryl Sulfate, Sucrose, Hydroxypropyl Methylcellulose, Copolymer Of Methacrylic Acid And Ethyl Acrylate (1:1), 30% Dispersion. The Composition Of The Gelatin Capsule Shell: Gelatin, Titanium Dioxide (E 171), Purified Water., Sterile Gauze Bandage Packaging No Less Than 5 M*10 Cm, Solution Of At Least 0.9% -200 Ml. Composition Of The Medicinal Product 1 Liter Of The Drug Contains Active Substance - Sodium Chloride 9.0 G, Excipient - Water For Injection., Childrens Spray At Least 112 Doses. Composition 1 Dose: Gramicidin C Dihydrochloride 0.0638 Mg, Which Corresponds To The Content Of Gramicidin C 0.03 Mg, Cetylpyridinium Chloride 0.1 Mg Excipients: Ethanol 96% - 9.5 Mg, Sucralose - 0.2 Mg, Glycerol - 33.2 Mg, Raspberry Flavor - 0.4 Mg, Citric Acid Monohydrate - 0.058 Mg, Sodium Citrate - 0.022 Mg, Polysorbate 80 - 0.4 Mg, Methyl Parahydroxybenzoate - 0.184 Mg, Propyl Parahydroxybenzoate - 0.02 Mg, Purified Water - Up To 0.2 Ml. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Eye Drops, Packaging Not Less Than 0.5%. 5 Mg/Ml. Composition Of The Medicinal Product 1 Ml Of Solution Contains: Active Substance - Levofloxacin Hemihydrate - 5.12 Mg (Equivalent To 5.0 Mg Of Levofloxacin); Excipients: Benzalkonium Chloride, Sodium Chloride, Hydrochloric Acid 1 M Or Sodium Hydroxide Solution 1 M, Water For Injection. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Drops Of At Least 30 Ml. Remaining Medicinal Product One Ml Of Drops For Oral Administration Contains Active Ingredient: At Least Simethicone 30 Mg Excipients: Macrogol Stearate, Glycerol Monostearate 40-55, Carbomers, Sodium Chloride, Sodium Citrate (E 331), Sucralose (E 955), Sodium Hydroxide (E 524), Sorbic Acid (E 200), Purified Water., Ophthalmic Ointment Not Less Than 3.5 G. Composition Of The Medicinal Product 1 G Ointment Contains Active Ingredients: Dexamethasone 1.0 Mg, Tobramycin 3.0 Mg Excipients: Anhydrous Chlorobutanol, Liquid Paraffin (Mineral Oil), White Petroleum Jelly. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Alcohol Solution For External Use, Not Less Than 1%. Composition Of The Medicinal Product 100 Ml Of The Drug Contains Active Substance: Chloramphenicol 1.0 G Excipient: Ethanol 70% Up To 100.0 Ml. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Capsules In Packaging No Less Than No. 10. Ingredients: Vitamin E (Alpha-Tocopherol Acetate) 100 Mg, Vegetable Oil (Sunflower Or Corn, Or Soy, Or Olive), Capsule Shell (Gelatin, Glycerol, Preservative Methyl Paragyl Roxybenzoate, Sugar Coloring), Vitamin A (Retinol Palmitate) 8600 Iu. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Tablets Of At Least 25 Mg No. 50. Composition: Active Substance - Baclofen 25 Mg; Excipients - Lactose, Potato Starch, Gelatin, Talc, Magnesium Stearate, Ethylcellulose. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Capsules, Packaging Of At Least 200 Mg No. 10. Composition Of The Medicinal Product One Capsule Contains Active Substance – Ibuprofen 200 Mg, Excipients: Macrogol 600, Potassium Hydroxide, Purified Water, Shell: Liquid Sorbitol, Non-Crystallizing, Liquid Maltitol, Gelatin. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Capsules Not Less Than 100 Mg No. 10. Pharmacotherapeutic Group Anti-Infective Drugs For Systemic Use. Antifungal Drugs For Systemic Use. Triazole Derivatives. Fluconazole. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Gel, In A Package Of At Least 10 G. Composition Of The Medicinal Product 1 G Of Gel Contains Active Ingredients: Lidocaine Hydrochloride, 20 Mg, Chamomile Flower Extract (1:4-5), 185 Mg, Excipients: Benzalkonium Chloride 50% Solution, Cinnamon Oil (Bark), Ceylon, Sodium Saccharin, Carbomers, Trometamol, Formic Acid, Ethanol 96%, Purified Water. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Tablets, Packaging Of At Least 200 Mg No. 20. Composition Of The Medicinal Product One Tablet Contains Active Substance – Acyclovir (In Terms Of 100% Substance) - 200 Mg, Excipients: Magnesium Stearate, Talc, Potato Starch. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Capsules Packaging Of At Least 2 Mg No. 10. Composition Of The Medicinal Product One Capsule Contains Active Substance – Loperamide Hydrochloride 2 Mg, Excipients: Magnesium Stearate, Corn Starch, Lactose Monohydrate, Capsule Shell Composition: Gelatin, Titanium Dioxide (E 171), Methyl Parahydroxybenzoate (E 218), Propyl Parahydroxybenzoate (E 216). The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Capsules Not Less Than 250 Mg No. 100 Capsules. Composition Of The Medicinal Product One 250 Mg Capsule Contains: Active Substance - Ursodeoxycholic Acid, 250 Mg Excipients: Corn Starch, Pregelatinized Corn Starch, Colloidal Anhydrous Silicon Dioxide, Magnesium Stearate. Shell Composition: Titanium Dioxide (E 171), Gelatin., Pasta At Least 30G. Composition Of The Medicinal Product 100 G Of The Drug Contains Active Substance – Zinc Oxide – 25 G Excipients – Potato Starch, Medical Vaseline. The Product And Shelf Life Must Comply With All Standards And Requirements Of Regulatory Documents For Monitoring The Quality And Safety Of Medicines And Medical Devices., Disposable Syringe No Less Than 20 Ml No. 1
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