GTR 116177376
Request For Quotation Purchase Of Medicines And Other Medical Products, According To The Customer’S Technical Specifications, Tel. 564008
ICB — International Competitive Bid
Closed
Central Asia
Tender Information
GTR Reference
116177376
Tendering Authority
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Tender No
17382517
Financer Name
Self-Funded
Work Title
Request For Quotation Purchase Of Medicines And Other Medical Products, According To The Customer’S Technical Specifications, Tel. 564008
Bid Type
ICB — International Competitive Bid
Country
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Geographical Region
Central Asia
Political Region
Commonwealth of Independent States, CIS
Last Date of Bid Submission
29-07-2026
Closed
Work Detail
Disposable Medical Gown. A Special Non-Woven Material Is Used For Their Manufacture. The Product Is Non-Toxic And Antistatic. The Fabric Of The Disposable Medical Product Has A High Degree Of Breathability And Is Resistant To Moisture. Sewn Evenly, Seams Without Gaps. Single Use, Non-Sterile. Sizes, Colors As Agreed (Standard, From 42 To More Than 52 Sizes)., Container For Collecting Biomaterials, At Least 125 Ml, Sterile, Solution For Injection, Not Less Than 0.5 Mg/Ml, 1 Ml. No. 10. Composition Of The Medicinal Product 1 Ml Of The Drug Contains Active Substance – Neostigmine Methyl Sulfate (Prozerin) 0.5 Mg, Excipients - Water For Injection., Elastic Medical Bandage Of High Extensibility, At Least 10 Cm X 5 M, 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., 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., 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., 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, 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., 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., 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., Tablets, No Less Than No. 100. Composition Of The Medicinal Product One Tablet Contains Active Substance – Ethamsylate 250 Mg, Excipients: Anhydrous Citric Acid, Corn Starch, Lactose Monohydrate, Povidone, Magnesium Stearate, Ethanol 96%*. 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, 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., 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., 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., 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.
Key Value
Tender Value
973,101 - KZT
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950f327b-353f-4e40-bfe2-06e1104630b0.html
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