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Acetylsalicylic Acid - 0.240 G, Paracetamol - 0.180 G, Caffeine In Terms Of Monohydrate 0.0300 G. Composition: One Tablet Must Contain Active Substances: Acetylsalicylic Acid - 0.240 G, Paracetamol -0.180 G, Caffeine In Terms Of Monohydrate 0.0300 G. Auxiliary Substances: Cocoa, Citric Acid, Potato Starch, Talc, Calcium Stearate. The Shelf Life Is At Least One Year From The Date Of Delivery Of The Goods. There Are 10 Tablets In 1 Blister., Ketoprofen Ampoule Solution. Solution For Injection 50 Mg (100 Mg) 2 Ml. There Are 10 Ampoules In A Package. 1 Ml Of Solution (1 Ampoule) Must Contain: Active Substance: Ketoprofen 50 Mg (100 Mg). Excipients: Propylene Glycol - 800 Mg, Ethanol - 200 Mg, Benzyl Alcohol - 40 Mg, Liquid Water - Up To 2 Ml. Shelf Life Is At Least One Year From The Date Of Delivery Of The Goods., Captopril Tablets. Pack Of 40 Pieces 50 Mg. Composition, Release Form And Packaging Active Substance: Captopril 50 Mg; Excipients: Ludipress Granulate (Lactose Monohydrate, Povidone, Crospovidone), Magnesium Stearate Or Lactose Monohydrate, Povidone, Crospovidone, Magnesium Stearate. The Shelf Life Is At Least One Year From The Date Of Delivery Of The Goods., Chloramphenicol Eye Drops. Eye Drops 0.25% -5 Ml. Composition: 5 Ml Of The Drug Contain The Active Substance Chloramphenicol - 12.5 Mg. Excipients: Boric Acid - 20.00 Mg, Purified Water - Up To 1.0 Ml. The Shelf Life Is At Least One Year From The Date Of Delivery Of The Goods., 100 Mg Tablets Ketoprofen. One Tablet Should Contain The Active Substance - Ketoprofen 100 Mg, Excipients: Lactose Monohydrate, Corn Starch, Povidone, Colloidal Anhydrous Silicon Dioxide, Talc, Magnesium Stearate, Film Coating Composition: Hypromelose, Macrogol 400, Indigotin (E 132), Titanium Dioxide (E 171), Talc, Carnauba Wax. There Are 20 Tablets In A Package. The Shelf Life Is At Least One Year From The Date Of Delivery Of The Goods., Ibuprofen Tablets. One Package Contains 20 Tablets. Composition Per Tablet - 200 Mg. Active Ingredient: Ibuprofen - 200 Excipients: Kollidon 90 F - 3.4 Mg; Microcrystalline Cellulose - 68 Mg; Talc - 6.8 Mg; Crospovidone (Kollidon Cl) - 10.2 Mg; Calcium Stearate - 3.4 Mg; Colloidal Silicon Dioxide (Aerosil) - 10.2 Mg; Corn Starch - 38.0 Mg; Shell: Hypromellose (Hydroxypropyl Methylcellulose) - 3.77 Mg; Talc - 0.41 Mg; Titanium Dioxide - 1.16 Mg; Propylene Glycol - 0.55 Mg; Macrogol-4000 (Polyethylene Glycol-4000, Polyethylene Oxide-4000) - 1.11 Mg. The Shelf Life Is At Least One Year From The Date Of Delivery Of The Goods., Melatonin Tablets. Tablets 3 Mg In A Package Of 24 Tablets, 1 Tablet: Active Ingredient: Melatonin 3 Mg. The Shelf Life Is At Least One Year From The Date Of Delivery Of The Goods., Paracetamol Tablets 0.5 G No. 10. Composition Per Tablet Active Substance: Paracetamol - 500 Mg; Excipients: Potato Starch, Croscarmellose Sodium (Croscarmellose Sodium), Povidone (Low Molecular Weight Medical Polyvinylpyrrolidone), Stearic Acid, Talc. No. 10 Tablets In 1 Blister. Indications Pain Syndrome Of Weak And Moderate Intensity (Arthralgia, Myalgia, Neuralgia, Migraine, Toothache And Headache, Algodysmenorrhea), Fever In Infectious And Inflammatory Diseases (Including Viral Infections). Shelf Life: At Least One Year., Nitroglycerin Tablets. 1 Tablet Should Contain: -Active Ingredient: Nitroglycerin 500 Mcg. Tablets Are White Or Almost White In Color With A Flat Surface, Scored And Chamfered. Pharmacological Action - Peripheral Vasodilating. Quantity Per Package: 40 Pcs. The Shelf Life Is At Least One Year From The Date Of Delivery Of The Goods., Acetylsalicylic Acid Tablets. Dosage Form Tablets 500 Mg Composition: One Tablet Should Contain: Active Substance - Acetylsalicylic Acid 500 Mg, Excipients: Potato Starch, Talc, Stearic Acid, Edible Citric Acid, Anhydrous Colloidal Silicon Dioxide. The Shelf Life Is At Least One Year From The Date Of Delivery Of The Goods. No. 10 Tablets In 1 Blister, Levomycin Tablets. There Are 10 Pcs In 1 Package. - Cellless Contour Packages. Composition: One Tablet Must Contain The Active Substance - Chloramphenicol 500.0 Mg, Excipients: Microcrystalline Cellulose 28.7 Mg, Hydroxypropyl Methylcellulose 6.5 Mg, Sodium Starch Glycolate 9.3 Mg, Calcium Stearate 5.5 Mg. The Shelf Life Is At Least One Year From The Date Of Delivery Of The Goods., Gel 50 G Ketoprofen. 100 G Of Gel Should Contain: Active Ingredient: Ketoprofen - 2.50 G. Excipients: Carbomer, Ethanol 96%, Neroli Flavor, Lavandin Flavor, Trolamine (Triethanolamine), Purified Water. The Shelf Life Is At Least One Year From The Date Of Delivery Of The Goods., Ibuprofen 5 G. The Gel Must Contain 50 G Of Active Substance: Ibuprofen 5 G; Excipients: Medium Chain Triglycerides, Purified Water, Glyceride Monostearate, Propylene Glycol, Macrogol-100-Stearate, Macrogol-30-Stearate, Xanthan Gum (Keltrol F), Sodium Methyl Parahydroxybenzoate, Lavender Oil, Orange Flower Oil (Nerol Oil). The Shelf Life Is At Least One Year From The Date Of Delivery Of The Goods., Methyl Salicylate 12.80 G, Racemic Menthol 5.91 G, Eucalyptus Oil 1.97 G, Turpentine Oil 1.47 G, Excipients. Cream For External Use Tube 67 Gr. Active Ingredients: Methyl Salicylate 12.80 G, Racemic Menthol 5.91 G, Eucalyptus Oil 1.97 G, Turpentine Oil 1.47 G, Excipients: Liquid Paraffin, Lanolin, Dovicyl 200, Cetostearyl Alcohol, Sodium Cetostearyl Sulfate, Propylene Glycol, Purified Water. The Shelf Life Is At Least One Year From The Date Of Delivery Of The Goods., Dimetindene Maleate 1 Mg. Gel In A Tube For External Use. 30 Gr. 1 G Of Gel Should Contain: Active Substance - Dimethindene Maleate 1 Mg. Excipients: Disodium Edetate - 50 Mg, Carbomer - About 900 Mg, Sodium Hydroxide (30% Solution) - About 1 G, Benzalkonium Chloride - 5 Mg, Propylene Glycol - 15 G, Purified Water - About 82.9 G. Shelf Life Is At Least A Year From The Moment Of Delivery Of The Goods., Heparin Sodium Gel. Gel For External Use In A Tube 50 G. Active Substance Heparin Sodium 100,000 Iu. Excipients: Carbomer 940 - 1.25 G, Methyl Parahydroxybenzoate - 0.12 G, Propyl Parahydroxybenzoate - 0.03 G, Ethanol 96% - 30 Ml, Neroli Oil - 0.05 G, Lavender Oil - 0.05 G, Trolamine (Triethanolamine) - 0.85 G, Purified Water - Up To 100 G. Shelf Life Is At Least One Year From The Date Of Delivery Of The Goods., Dioxomethyltetrahydropyrimidine (Methyluracil) - 40 Mg, Chloramphenicol - 7.5 Mg; Composition Of The Drug: Active Ingredients - Dioxomethyltetrahydropyrimidine (Methyluracil) - 40 Mg, Chloramphenicol - 7.5 Mg; Excipients - Macrogol-1500 - 190.5 Mg, Macrogol-400 - 762 Mg. The Shelf Life Is At Least One Year From The Date Of Delivery Of The Goods., Sodium Chloride 100 Ml (Saline Solution). Composition: 1 Ml Of Solution Should Contain: Active Substance - Sodium Chloride - 9 Mg Excipient - Water For Injection Theoretical Osmolarity - 308.0 Mosmol/L Description Colorless Transparent Liquid. Pharmacodynamics. Has A Detoxifying And Rehydrating Effect. Replenishes Sodium And Chlorine Deficiency In Various Pathological Conditions Of The Body And Temporarily Increases The Volume Of Fluid Circulating In The Vessels. The Shelf Life Is At Least One Year From The Date Of Delivery Of The Goods. 1 Bottle Contains 100 Ml., Ascorbic Acid Tablets No. 10. 10 Tablets In A Blister Pack Made Of Polyvinyl Chloride Film Or Unplasticized Pvc Film For Packaging Medicines And Flexible Packaging Based On Aluminum Foil, Or Printed Varnished Aluminum Foil, Or A Combination Material. One Tablet Should Contain Active Ingredients: Ascorbic Acid 100 Mg, Glucose Monohydrate 877 Mg. Excipients: Talc, Stearic Acid, Potato Starch. The Shelf Life Is At Least One Year From The Date Of Delivery Of The Goods., Nimesulide No. 30. Granules For The Preparation Of A Suspension For Oral Administration 2 G. The Sachet Should Contain 100 Mg Of Nimesulide. The Package Contains 30 Serving Sachets. Active Substance: Nimesulide 100 Mg. Excipients: Ketomacrogol 1000; Sucrose; Maltodextrin; Anhydrous Citric Acid; Orange Flavor. The Shelf Life Is At Least One Year From The Date Of Delivery Of The Goods., Glucose 200.0 Solution. Ingredients: 1 Liter Of Solution Should Contain Active Substance: Dextrose Monohydrate (Glucose, In Terms Of Anhydrous Dextrose) - 50.0 G Or 100.0 G Excipients: Sodium Chloride, 0.1 M Hydrochloric Acid, Water For Injection. Pharmacokinetics: It Is Completely Absorbed By The Body And Is Not Excreted By The Kidneys (Appearance In Urine Is A Pathological Sign). The Shelf Life Is At Least One Year From The Date Of Delivery Of The Goods. 1 Bottle 200 Ml
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