Request For Quotation Purchasing Medicines

15G Cream, A/V Betamethasone Dipropionate 0.64 Mg Equivalent To Betamethasone 0.50 Mg, Clotrimazole 10.00 Mg, Gentamicin Sulfate 2.25 Mg Equivalent To Gentamicin 1.00 Mg, I.V. Cetostearyl Alcohol, Cetomacrogol 1000, White Soft Paraffin, Light Paraffin Liquid, Propylene Glycol, Sodium Metabisulfite, Hydroxytoluene Butylate, Edta Disodium Salt, Disodium Hydrogen Phosphate, Sodium Dihydrogen Phosphate, Glyceryl Monostearate, Methylparaben, Propylparaben, Purified Water. 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., No. 50. Film-Coated Tablets, A/V-Iron (Ii) Sulfate Dry, 320 Mg (Equivalent To 100 Mg Of Iron (Ii)), Ascorbic Acid, 60 Mg, I/V-Povidone (K-25), Polyethene Powder, Carbomer 934 R, Magnesium Stearate. With An Expiration Date Of No Less Than December 2027. List 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., 3G No. 10. Powder For The Preparation Of A Suspension For Oral Administration, A/V - Dioctahedral Smectite (Diosmectite), 3 G, V/V - Sodium Saccharin, Glucose Monohydrate, Orange Flavor, Vanilla Flavor. 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., Fluconazole 150 Mg No. 1 Capsules 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., Pyridoxine Hydrochloride 5% 1Ml No. 10. Solution 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., Paracetamol 500 Mg No. 10. Pills. 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., 10 Mg No. 28. Film-Coated Tablets. A/V- Dapagliflozin Propanediol 12.30 Mg, Equivalent To 10 Mg Dapagliflozin. I/V- Microcrystalline Cellulose, Lactose Anhydrous, Crospovidone, Silicon Dioxide, Magnesium 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., 10 Mg/G 20 G. Dental Gel, A/V Metronidazole Benzoate 16 Mg (Equivalent To Metronidazole 10 Mg), Chlorhexidine Gluconate In The Form Of A 20% Solution 2.50 Mg (Equivalent To Chlorhexidine Gluconate 0.5 Mg), I.V. Propylene Glycol, Carbomer 980, Disodium Edetate, Saccharin, Levomenthol, Sodium Hydroxide, Purified Water. 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., Furosemide 10 Mg/Ml 2 Ml No. 10. Solution 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., No. 20. Tablets. A/V- Acetylsalicylic Acid – 0.240 G, Paracetamol – 0.180 G, Caffeine – 0.0300 G. I/V- Cocoa, Citric Acid, Potato Starch, Talc, Calcium Stearate. With An Expiration Date Of At Least December 2027. List Of Documents That Are Required When Receiving Medicines And Medical Products :Certificate Of Product Conformity (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., 10 Mg. No. 30 Tablets. A/V- Enalapril Maleate 10 Mg. I.V.- Lactose Anhydrous, Zinc 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., 0.5% 2Ml No. 10 Solution For Injection. A/V-Metoclopramide Hydrochloride 10.0 Mg (Calculated As An Anhydrous Substance). Iv - Sodium Sulfite, Sodium Chloride, Disodium Edetate, 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., 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., No. 21*3 (63) Film-Coated Tablets, A/V-Ethinyl Estradiol 0.03 Mg, Desogestrel 0.150 Mg, I/V- Α-Tocopherol, Magnesium Stearate, Colloidal Anhydrous Silicon Dioxide, Stearic Acid, Povidone K-30, Potato Starch, Lactose Monohydrate. 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., 10% 5Ml No. 10. Solution For Injection, A/V-Meldonium (In The Form Of Meldonium Dihydrate) 100 Mg, I.V. 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., 0.05% 100 Ml. Solution For External Use. A/V - 1 Ml Of The Drug: Chlorhexidine Digluconate 20% Solution - 0.0025 Ml, Purified Intravenous Water To 1 Ml. 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., 30G Pasta.A/V- Zinc Oxide - 25 G.V/V- Potato Starch, Medical Petroleum Jelly. With An Expiration Date Of No Less Than 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., 10 Mg No. 30. Tablets, A/V-Torasemide 10 Mg, I/V-Lactose Monohydrate, Corn Starch, Colloidal Silicon Dioxide, Magnesium Stearate. With An Expiration Date Of No Less Than December 2027. List Of Documents That Are Required When Receiving 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., 2Ml No. 10. Solution For Injection, A/V-Thiamine Hydrochloride 100 Mg, Pyridoxine Hydrochloride 100 Mg, Cyanocobalamin 1 Mg, I/V Lidocaine Hydrochloride 20 Mg, Benzyl Alcohol 40 Mg, Sodium Polyphosphate 20 Mg, Potassium Hexacyanoferrate (Iii) 0.20 Mg, Sodium Hydroxide 12 Mg, Water For Injections Up To 2 Ml. 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.