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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 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., 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., 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., Powder For Suspension, Not Less Than 100 Mg/5 Ml, 50 Ml. 1 Bottle Contains Cefixime Trihydrate (Micronized) 1.402 G. 5 Ml Of The Finished Suspension Contains 100 Mg Of Cefixime. 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 For The Preparation Of A Solution For Intravenous And Intramuscular Administration, Powder For Injection, At Least 1 G No. 1. Anti-Infective Drugs For Systemic Use. Antibacterial Drugs For Systemic Use. Beta-Lactam Antibacterial Drugs Are Different. Third Generation Cephalosporins. Ceftriaxone. 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 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., 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., Packaging Of At Least 250 Mg No. 20. Compound. One Tablet Contains Active Substance: Amoxicillin In The Form Of Amoxicillin Trihydrate 125 Mg, 250 Mg, 500 Mg, 1000 Mg Excipients: Dispersible Cellulose, Microcrystalline Cellulose, Crospovidone, Vanillin, Tangerine Flavor, Lemon Flavor, Saccharin, 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, Tablets, Packaging Of At Least 625 Mg No. 15. Composition One Film-Coated Tablet Contains The Active Ingredients: Amoxicillin (As Amoxicillin Trihydrate) 250 Mg And Clavulanic Acid (As Potassium Clavulanate) 125 Mg (For A Dosage Of 375 Mg) Or Amoxicillin (As Amoxicillin Trihydrate) 500 Mg And Clavulanic Acid (As Potassium Clavulanate) 125 Mg (For A Dosage Of 625 Mg); Excipients: Colloidal Silicon Dioxide, Crospovidone, Dried, Sodium Carboxymethylcellulose, Cross-Linked, Dried, Magnesium Stearate, Talc, Microcrystalline Cellulose, Dried; Film Shell Composition: Hydroxypropyl Cellulose, Ethyl Cellulose, Polysorbate, Triethyl Citrate, Titanium Dioxide (E 171), Talc. 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 250 Mg No. 6. Composition Of The Medicinal Product One Tablet Contains Active Substance - Azithromycin Dihydrate 262.02 Mg (Equivalent To Azithromycin 250 Mg), Excipients: Anhydrous Calcium Hydrogen Phosphate, Pregelatinized Starch (Starch 1500), Crospovidone, Polysorbate-80, Anhydrous Colloidal Silicon Dioxide, Microcrystalline Cellulose (Ph 112), Sodium Lauryl Sulfate, Talc, Magnesium Stearate, Shell Composition: Hypromellose (5 Cps), Titanium Dioxide (E171), Polyethylene Glycol. 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
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