Request For Quotation Acquisition Of Drugs

Salbutamol 100Mkg/Dose 200Doz 10Ml. Aerosol For Inhalation, Dosed. With A Shelf Life Of At Least December 2026. A List Of Documents That Are Necessary For The Receipt Of Medicines, Medical Devices: A Certificate Of Conformity Of Products (When Declared), Certifying That This Drug, Mi Has Passed Quality; Registration Certificate Of The Republic Of Kazakhstan, Certifying That This Drug Is Registered And Allowed For Use In The Territory Of The Republic Of Kazakhstan. If The Drug, The Medical Product Is Not Registered In The Republic Of Kazakhstan, Then A Permit For Import., Acetylsalicylic Acid 75 Mg, Tablets Covered With Intestinal Shell No. 30. Excipients: Corn Starch, Powder Cellulose, Sodium Carboxymethylcamal (Tibs). With A Shelf Life Of At Least December 2026. A List Of Documents That Are Necessary For The Receipt Of Medicines, Medical Devices: A Certificate Of Conformity Of Products (When Declared), Certifying That This Drug, Mi Has Passed Quality; Registration Certificate Of The Republic Of Kazakhstan, Certifying That This Drug Is Registered And Allowed For Use In The Territory Of The Republic Of Kazakhstan. If The Drug, The Medical Product Is Not Registered In The Republic Of Kazakhstan, Then A Permit For Import., Ammonia Solution 10% 20 Ml. Active Substance: Ammonia Concentrated Solution 40 Ml. Excipients: Water Purified To 100 Ml. With A Shelf Life Of At Least December 2026. A List Of Documents That Are Necessary For The Receipt Of Medicines, Medical Devices: A Certificate Of Conformity Of Products (When Declared), Certifying That This Drug, Mi Has Passed Quality; Registration Certificate Of The Republic Of Kazakhstan, Certifying That This Drug Is Registered And Allowed For Use In The Territory Of The Republic Of Kazakhstan. If The Drug, The Medical Product Is Not Registered In The Republic Of Kazakhstan, Then A Permit For Import., 2.4% 5Ml No. 5, Aminophylline (In Terms Of Dry Substance) 120.0 Mg, Injection Solution. With A Shelf Life Of At Least December 2026. A List Of Documents That Are Necessary For The Receipt Of Medicines, Medical Devices: A Certificate Of Conformity Of Products (When Declared), Certifying That This Drug, Mi Has Passed Quality; Registration Certificate Of The Republic Of Kazakhstan, Certifying That This Drug Is Registered And Allowed For Use In The Territory Of The Republic Of Kazakhstan. If The Drug, The Medical Product Is Not Registered In The Republic Of Kazakhstan, Then A Permit For Import., Ethinyl Estradiol 0.03 Mg, Deogestrel 0.15 Mg, No. 21*3 (63Tab.). Tablets Covered With A Film Membrane. Excipients: Α-Tocopherol, Magnesium Stearate, Silicon Dioxide Colloidal, Stearic Acid. With A Shelf Life Of At Least December 2026. A List Of Documents That Are Necessary For The Receipt Of Medicines, Medical Devices: A Certificate Of Conformity Of Products (When Declared), Certifying That This Drug, Mi Has Passed Quality; Registration Certificate Of The Republic Of Kazakhstan, Certifying That This Drug Is Registered And Allowed For Use In The Territory Of The Republic Of Kazakhstan. If The Drug, The Medical Product Is Not Registered In The Republic Of Kazakhstan, Then A Permit For Import., Methyluracil 10% Ointment 25G Auxiliary Substances: Vaselin Medical Emulsifier T-2, Purified Water. With A Shelf Life Of At Least December 2026. A List Of Documents That Are Necessary For The Receipt Of Medicines, Medical Devices: A Certificate Of Conformity Of Products (When Declared), Certifying That This Drug, Mi Has Passed Quality; Registration Certificate Of The Republic Of Kazakhstan, Certifying That This Drug Is Registered And Allowed For Use In The Territory Of The Republic Of Kazakhstan. If The Drug, The Medical Product Is Not Registered In The Republic Of Kazakhstan, Then A Permit For Import., 0.5G No. 10, Table. A/B Acid Acetylsalicylic - 0.5 G With A Shelf Life Of At Least December 2026. A List Of Documents That Are Necessary For The Receipt Of Medicines, Medical Devices: A Certificate Of Conformity Of Products (When Declared), Certifying That This Drug, Mi Has Passed Quality; Registration Certificate Of The Republic Of Kazakhstan, Certifying That This Drug Is Registered And Allowed For Use In The Territory Of The Republic Of Kazakhstan. If The Drug, The Medical Product Is Not Registered In The Republic Of Kazakhstan, Then A Permit For Import., 20 Mg No. 30, Tablets Covered With A Shell. A/In Atorvastatin 20 Mg In The Form Of Atorvastatin Calcium Salt. With A Shelf Life Of At Least December 2026. A List Of Documents That Are Necessary For The Receipt Of Medicines, Medical Devices: A Certificate Of Conformity Of Products (When Declared), Certifying That This Drug, Mi Has Passed Quality; Registration Certificate Of The Republic Of Kazakhstan, Certifying That This Drug Is Registered And Allowed For Use In The Territory Of The Republic Of Kazakhstan. If The Drug, The Medical Product Is Not Registered In The Republic Of Kazakhstan, Then A Permit For Import., 170Ml. Active Thing.- Aluminum Hydroxide Gel, Magnesium Hydroxide Pasta (Suspension For Oral Administration). In/In Sorbitol, Hydroxyethyl Cellulose, Methyl Parahydroxybenzoate, Propylparagexibenzoate, Butyl Parahydroxybenzoate, Sodium Sugar, Lemon Oil, Ethyl Alcohol 96%, Purified Water. With A Shelf Life Of At Least December 2026. A List Of Documents That Are Necessary For The Receipt Of Medicines, Medical Devices: A Certificate Of Conformity Of Products (When Declared), Certifying That This Drug, Mi Has Passed Quality; Registration Certificate Of The Republic Of Kazakhstan, Certifying That This Drug Is Registered And Allowed For Use In The Territory Of The Republic Of Kazakhstan. If The Drug, The Medical Product Is Not Registered In The Republic Of Kazakhstan, Then A Permit For Import., Basilbenzoate 20% 25G. Ointment In The Tube. A/B Gasylbenzoate 20.0 G. Trietanolamine Thermostabil (Trlamin) -5.0G, Stearic Acid -20.0 G, Macrogol 400 -5.0 G, The Water Purified To 100 G With An Expiration Date Is At Least December 2026. A List Of Documents That Are Necessary For The Receipt Of Medicines, Medical Devices: A Certificate Of Conformity Of Products (When Declared), Certifying That This Drug, Mi Has Passed Quality; Registration Certificate Of The Republic Of Kazakhstan, Certifying That This Drug Is Registered And Allowed For Use In The Territory Of The Republic Of Kazakhstan. If The Drug, The Medical Product Is Not Registered In The Republic Of Kazakhstan, Then A Permit For Import., 500Mkg/Ml 1Ml No. 10. Injection Solution. With A Shelf Life Of At Least December 2026. A List Of Documents That Are Necessary For The Receipt Of Medicines, Medical Devices: A Certificate Of Conformity Of Products (When Declared), Certifying That This Drug, Mi Has Passed Quality; Registration Certificate Of The Republic Of Kazakhstan, Certifying That This Drug Is Registered And Allowed For Use In The Territory Of The Republic Of Kazakhstan. If The Drug, The Medical Product Is Not Registered In The Republic Of Kazakhstan, Then A Permit For Import., 40Mg No. 100. Pills. A/In Drotaverine Hydrochloride, 40.0 Mg. With A Shelf Life Of At Least December 2026. A List Of Documents That Are Necessary For The Receipt Of Medicines, Medical Devices: A Certificate Of Conformity Of Products (When Declared), Certifying That This Drug, Mi Has Passed Quality; Registration Certificate Of The Republic Of Kazakhstan, Certifying That This Drug Is Registered And Allowed For Use In The Territory Of The Republic Of Kazakhstan. If The Drug, The Medical Product Is Not Registered In The Republic Of Kazakhstan, Then A Permit For Import., No. 10. Suppositories Rectal. A/In Heparin Sodium 1000 Iu (8.3 Mg), Anesthesin (Benzocaine) 50 Mg. With A Shelf Life Of At Least December 2026. A List Of Documents That Are Necessary For The Receipt Of Medicines, Medical Devices: A Certificate Of Conformity Of Products (When Declared), Certifying That This Drug, Mi Has Passed Quality; Registration Certificate Of The Republic Of Kazakhstan, Certifying That This Drug Is Registered And Allowed For Use In The Territory Of The Republic Of Kazakhstan. If The Drug, The Medical Product Is Not Registered In The Republic Of Kazakhstan, Then A Permit For Import., 5 Ml. Microcrystalline Suspension For Injection. A/In Hydrocortisone Aceta 125 Mg And Hydrochloride Of Monohydrate 26.66 Mg (Equivalent To Lidocaine Of Hydrochloride 25 Mg). With A Shelf Life Of At Least December 2026. A List Of Documents That Are Necessary For The Receipt Of Medicines, Medical Devices: A Certificate Of Conformity Of Products (When Declared), Certifying That This Drug, Mi Has Passed Quality; Registration Certificate Of The Republic Of Kazakhstan, Certifying That This Drug Is Registered And Allowed For Use In The Territory Of The Republic Of Kazakhstan. If The Drug, The Medical Product Is Not Registered In The Republic Of Kazakhstan, Then A Permit For Import., 5% 200Ml. A Solution For Infusions, A/In Glucose Anhydrous, 50.0 G. With A Shelf Life Of At Least December 2026. A List Of Documents That Are Necessary For The Receipt Of Medicines, Medical Devices: A Certificate Of Conformity Of Products (When Declared), Certifying That This Drug, Mi Has Passed Quality; Registration Certificate Of The Republic Of Kazakhstan, Certifying That This Drug Is Registered And Allowed For Use In The Territory Of The Republic Of Kazakhstan. If The Drug, The Medical Product Is Not Registered In The Republic Of Kazakhstan, Then A Permit For Import., 3% 100Ml. A Solution For External Use. With A Shelf Life Of At Least December 2026. A List Of Documents That Are Necessary For The Receipt Of Medicines, Medical Devices: A Certificate Of Conformity Of Products (When Declared), Certifying That This Drug, Mi Has Passed Quality; Registration Certificate Of The Republic Of Kazakhstan, Certifying That This Drug Is Registered And Allowed For Use In The Territory Of The Republic Of Kazakhstan. If The Drug, The Medical Product Is Not Registered In The Republic Of Kazakhstan, Then A Permit For Import., 50 Mg No. 50. Tablets Covered With A Shell. With A Shelf Life Of At Least December 2026. A List Of Documents That Are Necessary For The Receipt Of Medicines, Medical Devices: A Certificate Of Conformity Of Products (When Declared), Certifying That This Drug, Mi Has Passed Quality; Registration Certificate Of The Republic Of Kazakhstan, Certifying That This Drug Is Registered And Allowed For Use In The Territory Of The Republic Of Kazakhstan. If The Drug, The Medical Product Is Not Registered In The Republic Of Kazakhstan, Then A Permit For Import., 1% 50Ml. A Solution For External Use. A/V Iodine 0.01. In/In Potassium Iodide, Glycerin 85%, The Water Is Purified. With A Shelf Life Of At Least December 2026. A List Of Documents That Are Necessary For The Receipt Of Medicines, Medical Devices: A Certificate Of Conformity Of Products (When Declared), Certifying That This Drug, Mi Has Passed Quality; Registration Certificate Of The Republic Of Kazakhstan, Certifying That This Drug Is Registered And Allowed For Use In The Territory Of The Republic Of Kazakhstan. If The Drug, The Medical Product Is Not Registered In The Republic Of Kazakhstan, Then A Permit For Import., 550Mg No. 10. Tablets Covered With A Film Shell. A/V Of The Sodium 550 Mg. In/In Cellulose Microcrystalline Ph 101, Povidon K30, Talc, Magnesium Stearate, Purified Water. With A Shelf Life Of At Least December 2026. A List Of Documents That Are Necessary For The Receipt Of Medicines, Medical Devices: A Certificate Of Conformity Of Products (When Declared), Certifying That This Drug, Mi Has Passed Quality; Registration Certificate Of The Republic Of Kazakhstan, Certifying That This Drug Is Registered And Allowed For Use In The Territory Of The Republic Of Kazakhstan. If The Drug, The Medical Product Is Not Registered In The Republic Of Kazakhstan, Then A Permit For Import., Gentamycin 0.1% 15G. Ointment For External Use. With A Shelf Life Of At Least December 2026. A List Of Documents That Are Necessary For The Receipt Of Medicines, Medical Devices: A Certificate Of Conformity Of Products (When Declared), Certifying That This Drug, Mi Has Passed Quality; Registration Certificate Of The Republic Of Kazakhstan, Certifying That This Drug Is Registered And Allowed For Use In The Territory Of The Republic Of Kazakhstan. If The Drug, The Medical Product Is Not Registered In The Republic Of Kazakhstan, Then A Permit For Import.