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Suprastin Solution 20 Mg 1 Ml No. 5 (Chloropyramine), Suprastin®. International Nonproprietary Name: Chloropyramine Tablets, 25 Mg. Respiratory System. Antihistamines For Systemic Use. Substituted Ethylenediamines. Chloropyramine. Atx Code R06ac03. One Tablet Contains: Active Substance - Chloropyramine Hydrochloride, 25 Mg; Excipients: Lactose Monohydrate, Potato Starch, Sodium Carboxymethyl Starch (Type A), Talc, Gelatin, Stearic Acid. Description Of Appearance, Smell, Taste. 5 Amps Of Contour Cell Packaging In A Cardboard Box Along With Instructions For Medical Use In Kazakh And Russian. Shelf Life Is 5 Years. Do Not Use After The Expiration Date. Store At A Temperature Not Exceeding 25 ° C., Glucose Solution 5% 200 Ml. Glucose Solution For Infusion 5% And 10%, 100, 200, 250, 400 And 500 Ml. Blood And Hematopoietic Organs. Blood Substitutes And Perfusion Solutions. Solutions For Intravenous Administration. Preparations For Parenteral Nutrition. Carbohydrates. Glucose. Atc Code B05ba03. Composition Of The Medicinal Product: 1 Liter Of The Drug Contains; Active Substance - Anhydrous Glucose, 50.0 G Or 100.0 G; Excipient - Water For Injection. Description, Appearance, Smell, Taste. Colorless Transparent Liquid. 100, 200, 250, 400, 500 Ml Of The Drug Per Polypropylene Bottles With Graduations Of 100 (For A Volume Of 100 Ml), 200, 250 (For A Volume Of 200 And 250 Ml), 400 And 500 (For A Volume Of 400 And 500 Ml), With A Loop Holder, Sealed With Polypropylene Caps With A Rubber Lining And Equipped With A Cap With A Tear-Off Ring For Opening, Welded On Bottle., Acetylsalicylic Acid 500 Mg No. 10. Acetylsalicylic Acid Tablets 0.5 G. Nervous System. Analgesics. Other Analgesics And Antipyretics. Salicylic Acid And Its Derivatives. Acetylsalicylic Acid. Atx Code N02ba01. One Tablet Contains: Active Substance: Acetylsalicylic Acid - 0.5 G; Excipients: Citric Acid, Potato Starch, Talc. Description Of Appearance, Smell, Taste. White Tablets, Slightly Marbled, Odorless Or With A Weak Characteristic Odor, Flat-Cylindrical With A Score And A Bevel. 10 Tablets Are Placed In A Blister Pack Made Of Polyvinyl Chloride Film And Printed Aluminum Foil Varnished., Platiphylline Hydrotartrates Composition: 1 Ml Of The Drug Contains Platiphylline Hydrotartrate 2 Mg; Water For Injection. Description Of Appearance, Smell, Taste. Transparent, Colorless Liquid. Release Form And Packaging 1 Ml Of The Drug In Glass Ampoules. The Text Of The Marking Is Applied To The Ampoule Using Intaglio Printing Or A Self-Adhesive Label Is Affixed. 10 Ampoules, Along With Instructions For Medical Use In Kazakh And Russian And A Ceramic Cutting Disc Or Ceramic Ampoule Knife, Are Placed In A Box With Partitions. Terms Of Release From Pharmacies According To The Recipe., Nitroglycerin Tablets 0.5 Mg No. 40.0.5 Mg. One Tablet Contains The Active Substance: Nitroglycerin 2% On Lactose, In Terms Of Nitroglycerin 0.5 Mg; Excipients: Lactose Monohydrate, Povidone 25, Microcrystalline Cellulose, Croscarmellose Sodium, Magnesium Stearate. Single-Layer Tablets Of Round Shape, With Flat Top And Bottom Surfaces, The Edges Of Which Are Beveled, With A Streak, White Or Almost White. Marbling Is Allowed On The Surface Of The Tablets. A Relatively Homogeneous Structure Is Visible On The Fault Under A Magnifying Glass. Vasodilators, For The Treatment Of Heart Diseases Organic Nitrates. Nitroglycerine. Atx Code C01d A02. Sublingual Tablets 0.5 Mg. 40 Tablets In A Polymer Container. Each Container, Along With Instructions For Medical Use In The State And Russian Languages, Is Placed In A Cardboard Pack. Shelf Life 2 Years, Prednisolone Solution 30 Mg/1 Ml No. 3. Prednisolone Solution For Intravenous And Intramuscular Administration, 30 Mg/Ml. Code Atc H02ab06. 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, Orthophosphoric Acid, Water For Injection. Transparent Solution, Colorless Or With A Greenish-Yellow Tint. 1 Ml Each The Drug Is Placed In A Dark Glass Ampoule. 3 Ampoules Are Placed In A Plastic Tray Or In A Blister Pack Made Of Aluminum Foil And Transparent Pvc Film. A Plastic Tray Or Blister Pack, Together With Instructions For Medical Use In Kazakh And Russian, Are Placed In A Cardboard Box, Ascorbic Acid Solution 5% 2Ml No. 10, Ascorbic Acid Solution For Intravenous And Intramuscular Administration, 50 Mg/Ml. Pharmacotherapeutic Group: Digestive Tract And Metabolism. Vitamins. Ascorbic Acid (Vitamin C), Including Combinations. Ascorbic Acid In Its Pure Form. Ascorbic Acid. Atx Code A11ga01 Composition Of The Medicinal Product: Active Substance - Ascorbic Acid, 50.0 G; Excipients - Sodium Bicarbonate (Sodium Bicarbonate) - 23.85 G, Anhydrous Sodium Sulfite (Sodium Sulfite) -2.0 G, Water For Injection - Up To 1 L. Description Of Appearance, Smell, Taste. Transparent, Slightly Colored Liquid. 2 Ml In Neutral Glass Ampoules. 10 Ampoules Along With Instructions For Medical Use In Kazakh And Russian With A Knife For Opening Ampoules Or An Ampoule Scarifier In A Cardboard Box., Sterile Latex Medical Gloves, Size 7-8, Calcium Chloride Solution 10% 5 Ml No. 5. Calcium Chloride Solution For Injection 10%, 5 Ml. Composition 5 Ml Solution Contains The Active Substance - Calcium Chloride Hexahydrate 500 Mg, Excipient - Water For Injection. Description: Transparent Colorless Liquid Pharmacotherapeutic Group Plasma Replacement And Perfusion Solutions. Electrolyte Solutions. Calcium Chloride. Atx Code B05ха07, Paracetamol Tablets 500 Mg No. 10, Paracetamol Tablets, 500 Mg. Nervous System. Analgesics. Other Analgesics And Antipyretics. Anilides. Paracetamol. Atc Code N02be01. One Tablet Contains: Active Substance - Paracetamol 500 Mg, Excipients: Potato Starch, Povidone K30, Carboxymethylcellulose Sodium Salt, Calcium Stearate. Tablets Are Round, White, With A Flat Surface, With A Chamfer And A Score. 10 Tablets Each In A Contour-Free Packaging Made Of Packaging Paper With A Polymer Coating With Two Sides. 250 Contour Cellless Packages Together With Instructions For Medical Use In Kazakh And Russian Are Placed In A Cardboard Box (Multiple Packaging)., No-Spa Tablets 40 Mg No. 24 (Drotoverine), International Nonproprietary Name Drotaverine. Dosage Form Tablets, 40 Mg. Composition One Tablet Contains: Active Substance - Drotaverine Hydrochloride 40.0 Mg, Excipients: Lactose Monohydrate, Corn Starch, Povidone, Magnesium Stearate, Talc. Description Tablets Are Round In Shape With A Biconvex Surface, Yellow In Color With A Greenish Or Orange Tint, Engraved “Spa” On One Side, With A Diameter Of About 7 Mm And A Height Of About 3.4 Mm. Pharmacotherapeutic Group Drugs For The Treatment Of Functional Intestinal Disorders. Papaverine And Its Derivatives. Drotaverine. Or 24 Tablets Are Placed In Blister Packs Made Of Polyvinyl Chloride Film And Aluminum Foil. 1 Contour Package Along With Instructions For Medical Use In The State And Russian Languages Is Placed In A Cardboard Pack. Atx Code A03ad02, Salbutamol Aerosol 100 Mcg/Dose, 200 Doses, Salbutamol Aerosol For Inhalation, Dosed, 100 Mcg/Dose, 200 Doses. Homogeneous White Suspension. Preparations For The Treatment Of Diseases Of The Respiratory System. Drugs For The Treatment Of Obstructive Airway Diseases. Inhalation Sympathomimetics. Beta 2—Selective Adrenergic Agonists. Salbutamol.Atc Code R03ac02
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