Ascorbic Acid 5% 2Ml No. 10. Solution For Intravenous And Intramuscular Administration. 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., 667 G/L 1000 Ml. Syrup. A/V-Lactulose Liquid 667 G/L. 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., 10Mg/Ml 5Ml. Eye Drops. A/V-Brinzolamide 10 Mg. Iv Benzalkonium Chloride 50% Solution, Disodium Edetate, Sodium Chloride, Tyloxapol, Mannitol, Carbomer (974P), Sodium Hydroxide And/Or Hydrochloric Acid For Ph Correction, Sterile Purified Water 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., 250 Mg 2 Ml No. 10. Solution For Injection, A/V-Ethamsylate 250 Mg, I/V-Sodium Metabisulfite, Sodium Bicarbonate, Water For Injection, Nitrogen. 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., 0.1% 15 G. Ointment For External Use, A/V-Gentamicin Sulfate (In Terms Of Gentamicin) - 0.1 G, I/V-Solid Petroleum Paraffin - 5.0 G, Medical Petroleum Jelly - Up To 100. 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 (If Declaration), Certifying That This Drug, Medical Device Has Passed A Quality Assessment; Registration Certificate Of The Republic Of Kazakhstan, Certifying That This Drug, Medical Device Is Registered And Approved For Use In The Territory Of The Republic Of Kazakhstan. If The Medical Device Is Not Registered In The Republic Of Kazakhstan, An Import Permit Is Required., 4% Inibsa With Epinephrine 1:100,000 1.8 Ml No. 100. Solution For Injection In Cartridges. A/V - Articaine Hydrochloride 40.0 Mg, Epinephrine Bitartrate 0.018 Mg (Equivalent To Epinephrine 0.010 Mg). I/V - Sodium Chloride, Sodium Metabisulfite, Citric Acid Monohydrate, 2M Sodium Hydroxide Solution, 2M Hydrochloric Acid, 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., 24 Mg No. 30. Tablets, A/V-Betagistine Dihydrochloride 24 Mg, A/V-Microcrystalline Cellulose Ph 112, Mannitol, Anhydrous Citric Acid, Colloidal Silicon Dioxide (Aerosil 200), Stearic Acid, Talc. With An Expiration Date Of At Least December 2027. List Of Documents That Are Required When Receiving Medicines And Medical Devices: Certificate Of Product Conformity (Upon Declaration), Certifying That The Drug Or Medical Device Has Passed The Quality Assessment; Registration Certificate Of The Republic Of 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/Ml 5 Ml No. 10. Solution For Intracavitary And External Use, A/V - Hydroxymethylquinoxaline Dioxide (Dioxidine) - 10.0 Mg, I/V - Water For Injection - Up 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., Captopril 25 Mg No. 30. 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., Heparin Ointment 25G. Ointment For External Use. 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., 1% 80G. External Gel, A/V-Progesterone Micronized 1 G, I/V-Octyldodecanol, Carbomer (Carbopol ® 980 Nf), Macroglycerol Hydroxystearate, Trolamine (Or Triethanolamine), Ethanol 96%, 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., Nitroxoline 50 Mg No. 50. Film-Coated Tablets. 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., 2.4% 5Ml No. 10. Solution For Injection. A/V-Aminophylline (In Terms Of Dry Matter) 120.0 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., 13.5 Mg No. 500. Tablets, A/B-Calcium Sennoside 15% (Equivalent To 13.5 Mg Of Senna Calcium Salts Of Sennosides A And B), 90.00 Mg, A/V- Lactose, Corn Starch, Microcrystalline Cellulose, Purified Talc, Methyl Parahydroxybenzoate, Magnesium Stearate, Sodium Lauryl Sulfate, Sodium Carmellose With An Expiration Date Of No Less Than December 2027. List Of Documents Required For The Receipt Of Medicines And Medical Devices: 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., 1% 50 Ml. Solution For External Use, A/V-Iodine 0.01 G, A/V- Potassium Iodide, Glycerin 85%, Purified Water. With An Expiration Date Of No Less Than December 2027. List Of Documents That Are Required When Receiving Medicines, Medical Devices: 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., Diclofenac 100 Mg No. 10. Suppositories. 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., Lidocaine 2% 2Ml 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., Tetracycline 3% 15G Ointment. 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., 40 G. Liniment For External Use. A/C - Birch Tar - 1.2 G, Xeroform - 1.2 G In Terms Of Bismuth Oxide 0.599 G, W/W - Colloidal Anhydrous Silicon Dioxide, Castor Oil. 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., A/B- One Red Pill Contains: Retinol Palmitate (Vitamin A) Concentrate (Synthetic, Oil Form) 1.7 Million Iu/G (Equivalent To Vitamin A) 2.94 Mg (5000 Iu), Cholecalciferol Concentrate (Oil Form) 1 Million Iu/G (Equivalent To Vitamin D3) 0.20 Mg (200 Iu), Acid Ascorbic Acid (Vitamin C) 60.00 Mg, Thiamine Nitrate (Vitamin B1) 1.00 Mg, Riboflavin (Vitamin B2) 1.20 Mg, Pyridoxine Hydrochloride (Vitamin B6) 2.00 Mg, Cyanocobalamin 0.1% In Mannitol (Vitamin B12) 3.00 Mg, Nicotinamide (Vitamin Pp) 13.00 Mg, Folic Acid (Vitamin B9) 0.40 Mg, Calcium Pantothenate (Vitamin B5) 5.00 Mg, Alpha-Tocopherol Acetate (Vitamin E) 10.00 Mg. One Blue Pellet Contains: Calcium Hydrogen Phosphate Dihydrate (Equivalent To Calcium) (Equivalent To Phosphorus) 64.50 Mg (15.00 Mg) (12.00 Mg), Iron Fumarate (Equivalent To Iron) 30.30 Mg (10.00 Mg), Copper Sulfate Pentahydrate (Equivalent To Copper) 4.00 Mg (1.00 Mg), Zinc Sulfate Heptahydrate (Equivalent To Zinc) 13.30 Mg (3.00 Mg), Magnesium Lactate Dihydrate (Equivalent To Magnesium) 200.00 Mg (20.00 Mg), Manganese Sulfate Monohydrate (Equivalent To Manganese) 3.10 Mg (1.00 Mg), Sodium Molybdate Dihydrate (Equivalent To Molybdenum) 0.25 Mg (0.10 Mg). 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.
