Request For Quotation Purchasing Medicines in Kazakhstan

Work Detail

500 Mg No. 60. Capsules, A/V-Meldonium Dihydrate 500 Mg, I/V- Potato Starch, Colloidal Silicon Dioxide, Calcium Stearate. With An Expiration Date Of At Least December 2027. List Of Documents That Are Required Upon Receipt Of Medicines, Medical Devices: Certificate Of Conformity Of Products (When Declaring), Certifying That This Drug Or Medical Device Has Passed A Quality Assessment; Registration Certificate Of The Republic Kazakhstan, Certifying That This Drug Or Medical Device Is Registered And Approved For Use On The Territory Of The Republic Of Kazakhstan. If The Drug If The Medical Device Is Not Registered In The Republic Of Kazakhstan, An Import Permit Is Required., 50Mg/4Mg 2Ml No.6. Solution For Intramuscular Injection, A/V - Dexketoprofenatrometamol 73.8 Mg (Equivalent To Dexketoprofen 50.0 Mg) And Thiocolchicoside 4.0 Mg, I/V - Sodium Chloride, Ethyl Alcohol 96%, Sodium Hydroxide, Water For Injection. With An Expiration Date Of At Least December 2027. List Of Documents That Are Required Upon Receipt Of Medicines, Medical Devices: Certificate Of Conformity Of Products (When Declaring), Certifying That This Drug Or Medical Device Has Passed A Quality Assessment; Registration Certificate Of The Republic Kazakhstan, Certifying That This Drug Or Medical Device Is Registered And Approved For Use On The Territory Of The Republic Of Kazakhstan. If The Drug If The Medical Device Is Not Registered In The Republic Of Kazakhstan, An Import Permit Is Required., 250 Mg No. 14. Tablets, A/V-Terbinafine Hydrochloride 281.25 Mg (Equivalent To Terbinafine 250.00 Mg), Intravenous - Hydroxypropyl Methylcellulose, Sodium Starch Glycolate, Microcrystalline Cellulose, Colloidal Silicon Dioxide, Magnesium Stearate. With An Expiration Date Of No Less Than December 2027. List Of Documents, Which Are Necessary Upon Receipt Of Medicines, Medical Devices: Certificate Of Conformity Of Products (When Declaring), Certifying That This Drug Or Medical Device Has Passed A Quality Assessment; Registration Certificate Of The Republic Kazakhstan, Certifying That This Drug Or Medical Device Is Registered And Approved For Use On The Territory Of The Republic Of Kazakhstan. If The Drug If The Medical Device Is Not Registered In The Republic Of Kazakhstan, An Import Permit Is Required.

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