Request For Quotation Purchase Of Medicines And Other Medical Products, According To The Customer’S Technical Specifications, Tel. 564008

Tablets Not Less Than 20 Mg No. 10. Composition One Tablet Contains Active Substance – Furatsilina 0.02 G Excipient – Sodium Chloride, Syrup, Packaging Of At Least 100 Ml. Composition 5 Ml Of Syrup Contains: Active Substances: Tribulus Terrestris Extract 91 Mg Boerhavia Spreading Roots Extract 67Mg Saxifraga Ligulate Roots Extract 53 Mg Almond Ground Tuber Extract 42 Mg Asparagus Racemosus Root Extract 21 Mg Fire Bean Seed Extract 21Mg Vetiver Root Extract 21 Mg Turmeric Zedoaria Rhizome Extract 14Mg Trikatu Rhizomes And Fruits Extract 20 Mg Potassium Nitrate 42.5 Mg Ammonium Chloride 2.5 Mg Potassium Carbonate 5Mg Sodium Chloride 50 Mg Excipients: Sugar S30, Sorbitol 70%, Sun 528 Flavor, Citric Acid, Sodium Citrate, Sodium Methyl Parahydroxybenzoate, Sodium Propyl Parahydroxybenzoate, Sodium Benzoate, Qs 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, 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., 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., 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., 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 Of At Least 10 Mg No. 50. Composition: Active Substance - Baclofen 10 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., 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., 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., 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., 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.