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Trigrim 10 Mg, Tablets, No. 30. Dosage Form: Tablets. Composition: One Tablet Contains: Active Ingredient: Torasemide - 10 Mg. Excipients: Lactose Monohydrate, Corn Starch, Colloidal Silicon Dioxide, Magnesium Stearate.International Nonproprietary Name: Torasemide. Pharmacotherapeutic Group: Drugs For The Treatment Of Diseases Of The Cardiovascular System. Diuretics. Highly Active Diuretics. Sulfonamides. Atc Code: C03ca04. Description: White Tablets, Round, Flat, Scored. Packaging: 10 Tablets In A Blister Pack. 3 Blister Packs Together With Instructions For Medical Use In Kazakh And Russian Are Placed In A Cardboard Box. Quantity: According To The Customer’S Request. Quality Requirements: The Drug Must Have A Valid State Registration In The Republic Of Kazakhstan. The Quality Of The Drug Must Correspond To The Approved Instructions For Medical Use. The Drug Must Be New, In The Original Factory Packaging, Without Damage. Labeling Must Contain Name Of The Drug, Dosage, Series, Date Of Manufacture And Expiration Date. The Drug Must Be Accompanied By Documents Confirming The Quality And Compliance With The Requirements Of The Legislation Of The Republic Of Kazakhstan. The Remaining Shelf Life At The Time Of Delivery Must Be At Least 12 Months, Unless A Different Period Is Agreed By The Customer. Terms Of Delivery: Delivery Is Carried Out To The Customer’S Location.Shipping, Loading And Unloading Costs Are Borne By The Supplier. The Product Is Shipped In Its Original Factory Packaging., Preductal Od 80 Mg, Capsules With Prolonged Release, No. 60. Dosage Form: Capsules With Prolonged Release. Composition: One Capsule Contains: Active Ingredient: Trimetazidine Dihydrochloride - 80 Mg.Excipients: Sugar Spheres (Sucrose And Corn Starch), Hypromellose, Ethylcellulose, Tributylacetyl Citrate, Talc, Magnesium Stearate. Capsule Shell: Gelatin, Titanium Dioxide, Red Iron Oxide. International Nonproprietary Name: Trimetazidine. Pharmacotherapeutic Group: Drugs For The Treatment Of Diseases Of The Cardiovascular System. Other Drugs For The Treatment Of Heart Disease. Trimetazidine.Atc Code: C01eb15.Description: Hard Gelatin Capsules No. 2 With A White Body And An Orange-Red Cap. The Manufacturers Logo And The Number “80” Are Printed In White On The Lid. The Contents Of The Capsules Are Spherical Granules Coated From White To Almost White. Packaging: 60 Capsules In One Package. Quantity: According To The Customer’S Request. Quality Requirements: The Drug Must Have Valid State Registration In The Republic Of Kazakhstan. The Quality Of The Drug Must Comply With The Approved Instructions For Medical Use. The Drug Must Be New, In The Original Factory Packaging, Without Damage. Labeling Must Contain The Name Of The Drug, Dosage, Series, Date Of Manufacture And Expiration Date. The Drug Must Be Accompanied By Documents Confirming The Quality And Compliance With The Requirements Of The Legislation Of The Republic Of Kazakhstan. The Remaining Shelf Life At The Time Of Delivery Must Be At Least 12 Months, Unless A Different Period Is Agreed By The Customer. Terms Of Delivery: Delivery Is Carried Out To The Customer’S Location.Shipping, Loading And Unloading Costs Are Borne By The Supplier. The Product Is Shipped In Its Original Factory Packaging., Ursodex 250 Mg, Capsules, No. 50. Dosage Form: Capsules. Composition: One Capsule Contains: Active Ingredient: Ursodeoxycholic Acid - 250 Mg. Excipients: According To The Approved Instructions For Medical Use.International Nonproprietary Name: Ursodeoxycholic Acid. Pharmacotherapeutic Group: Drugs For The Treatment Of Diseases Of The Liver And Biliary Tract. Bile Acid Preparations. Ursodeoxycholic Acid. Atc Code: A05aa02.Description: White Hard Gelatin Capsules. The Contents Of The Capsules Are White Or Almost White Powder. Packaging: 50 Capsules In One Package. Outline Blister Packs Are Placed In A Cardboard Box Along With Instructions For Medical Use.Quantity: According To The Customer’S Request. Quality Requirements: The Drug Must Have A Valid State Registration In The Republic Of Kazakhstan. The Quality Of The Drug Must Correspond To The Approved Instructions For Medical Use. The Drug Must Be New, In The Original Factory Packaging, Without Damage. Labeling Must Contain The Name Of The Drug, Dosage, Series, Date Of Manufacture And Expiration Date. The Drug Must Be Accompanied By Documents Confirming The Quality And Compliance With The Requirements Of The Legislation Of The Republic Of Kazakhstan. Remaining Period Shelf Life At The Time Of Delivery Must Be At Least 12 Months, Unless A Different Period Is Agreed By The Customer. Terms Of Delivery: Delivery Is Carried Out To The Customers Location. The Costs Of Delivery, Loading And Unloading Are Borne By The Supplier. The Goods Are Supplied In The Original Factory Packaging., Isoket, Dosed Spray 1.25 Mg/Dose, 15 Ml. Dosage Form: Dosed Spray. Composition: 100 G Of The Drug Contains:Active Ingredient: Isosorbide Dinitrate - 2.946 G. Excipients: Macrogol 400, Ethanol 100%.International Nonproprietary Name: Isosorbide Dinitrate. Pharmacotherapeutic Group: Vasodilators For The Treatment Of Heart Diseases. Organic Nitrates. Isosorbide Dinitrate. Atc Code: C01da08. Description: Transparent, Colorless Solution With A Characteristic Odor Of Alcohol. Packaging: 15 Ml Of The Drug (300 Doses) In A Dark Glass Bottle With A Dosing Device And A Protective Cap. 1 Bottle Together With Instructions For Medical Use In Kazakh And Russian Are Placed In A Cardboard Box. Quantity: According To The Customer’S Request. Quality Requirements: The Drug Must Have A Valid State Registration In The Republic Of Kazakhstan. The Quality Of The Drug Must Correspond To The Approved Instructions For Medical Use.The Drug Must Be New, In The Original Factory Packaging, Without Damage. The Labeling Must Contain The Name Of The Drug, Dosage, Series, Date Of Manufacture And Expiration Date. The Drug Must Be Accompanied By Documents Confirming The Quality And Compliance With The Requirements Of The Legislation Of The Republic Of Kazakhstan. The Remaining Shelf Life At The Time Of Delivery Must Be At Least 12 Months, Unless A Different Period Is Agreed By The Customer. Terms Of Delivery: Delivery Is Carried Out To The Customer’S Location. The Costs Of Delivery, Loading And Unloading Are Borne By Supplier. The Product Is Supplied In Original Factory Packaging., Neladex-Ns, Nasal Spray, 15 Ml. Dosage Form: Nasal Spray. Composition: 1 Ml Of The Drug Contains: Dexamethasone Sodium Metasulfobenzoate - 0.250 Mg. Phenylephrine Hydrochloride - 2.500 Mg. Neomycin Sulfate - 8.387 Mg (6500 Iu). Polymyxin B Sulfate - 1.256 Mg (10000 Iu). Pharmacotherapeutic Group: Drugs For The Treatment Of Diseases Of The Respiratory System. Nasal Preparations For Topical Use. Decongestants And Other Nasal Preparations For Topical Use. Atc Code: R01ad53. Description: Transparent Yellowish Solution. Packaging: 15 Ml Of The Drug In A Dark Glass Bottle With A Dosing Device, A Protective Cap And A Protective Ring. 1 Bottle Together With Instructions For Medical Use In Kazakh And Russian Are Placed In A Cardboard Box. Quantity: According To The Customer’S Request. Quality Requirements: The Drug Must Have Valid State Registration In The Republic Of Kazakhstan. The Quality Of The Drug Must Correspond To The Approved Instructions For Medical Use. The Drug Must Be New, In The Original Factory Packaging, Without Damage.Labeling Must Contain The Name Of The Drug, Volume, Series, Date Of Manufacture And Expiration Date.The Drug Must Be Accompanied By Documents Confirming The Quality And Compliance With The Requirements Of The Legislation Of The Republic Of Kazakhstan. The Remaining Shelf Life At The Time Of Delivery Must Be At Least 12 Months, Unless A Different Period Is Agreed By The Customer.Terms Of Delivery: Delivery Is Carried Out To The Customers Location. The Costs Of Delivery, Loading And Unloading Are Borne By The Supplier.The Product Is Supplied In Original Factory Packaging. Delivery To The Customer, Ranoprost 0.4 Mg, Capsules, No. 30. Dosage Form: Modified Release Capsules. Composition: One Capsule Contains:Active Ingredient: Tamsulosin Hydrochloride - 0.4 Mg (In Terms Of Tamsulosin). Pharmacotherapeutic Group: Drugs For The Treatment Of Urological Diseases. Drugs For The Treatment Of Benign Prostatic Hyperplasia. Alpha Blockers. Atc Code: G04ca02. Description: Modified-Release Capsules, Intended For Oral Use. Packaging: 30 Capsules In One Package. Quantity: According To The Customer’S Request. Quality Requirements: The Drug Must Have A Valid State Registration In The Republic Of Kazakhstan. The Quality Of The Drug Must Comply With The Approved Instructions For Medical Use. The Drug Must Be New, In Original Factory Packaging, Without Damage. Labeling Must Contain The Name Of The Drug, Dosage, Series, Date Of Manufacture And Expiration Date.The Drug Must Be Accompanied By Documents Confirming The Quality And Compliance With The Requirements Of The Legislation Of The Republic Of Kazakhstan. The Remaining Shelf Life At The Time Of Delivery Must Be At Least 12 Months, Unless A Different Period Is Agreed By The Customer.Terms Of Delivery: Delivery Is Carried Out To The Customers Location. The Costs Of Delivery, Loading And Unloading Are Borne By The Supplier.The Product Is Supplied In Original Factory Packaging., Betaserc 24 Mg, Tablets, No. 20. Dosage Form: Tablets. Composition: One Tablet Contains: Active Ingredient: Betahistine Dihydrochloride - 24 Mg. Excipients: Microcrystalline Cellulose, Mannitol, Citric Acid Monohydrate, Colloidal Anhydrous Silicon Dioxide, Talc. Pharmacotherapeutic Group: Drugs For The Treatment Of Diseases Of The Nervous System. Remedies For Dizziness. Betahistine. Atc Code: N07ca01. Description: Tablets Are Round, Biconvex, White Or Almost White, With A Chamfer, A Score On One Side And The Marking “289” On Both Sides Of The Score. Packaging: 20 Tablets In A Blister Pack. 1 Package Together With Instructions For Medical Use In Kazakh And Russian Are Placed In A Cardboard Box. Quantity: According To The Customer’S Request. Quality Requirements: The Drug Must Have Valid State Registration In The Republic Of Kazakhstan. The Quality Of The Drug Must Correspond To The Approved Instructions For Medical Use. The Drug Must Be New, In The Original Factory Packaging, Without Damage.Labeling Must Contain The Name Of The Drug, Dosage, Series, Date Of Manufacture And Expiration Date.The Drug Must Be Accompanied By Documents Confirming The Quality And Compliance With The Requirements Of The Legislation Of The Republic Of Kazakhstan. The Remaining Shelf Life At The Time Of Delivery Must Be At Least 12 Months, Unless Another Period Is Agreed By The Customer. Delivery Conditions: Delivery Is Carried Out To The Customer’S Location. The Costs Of Delivery, Loading And Unloading Are Borne By The Supplier. The Product Is Supplied In The Original Factory Packaging. Delivery To The Customer, Troxevasin, Gel For External Use 2%, 100 G. Dosage Form: Gel For External Use 2%. Composition: 100 G Of Gel Contains: Active Ingredient: Troxerutin - 2 G. Excipients: Carbomer, Disodium Edta, Benzalkonium Chloride, Triethanolamine, Purified Water. Pharmacotherapeutic Group: Drugs, Reducing Capillary Permeability. Bioflavonoids.Atx Code: C05ca04. Description: Homogeneous Gel From Yellow To Light Brown Color. Packaging: 100 G Of Gel In An Aluminum Or Laminated Tube. 1 Tube Together With Instructions For Medical Use In Kazakh And Russian Are Placed In A Cardboard Box. Quantity: According To The Customer’S Request. Quality Requirements: The Drug Must Have Valid State Registration In The Republic Of Kazakhstan. The Quality Of The Drug Must Comply With The Approved Instructions For Medical Use.The Drug Must Be New, In The Original Factory Packaging, Without Damage. The Labeling Must Contain The Name Of The Drug, Dosage, Series, Date Of Manufacture And Expiration Date. The Drug Must Be Accompanied By Documents Confirming The Quality And Compliance With The Requirements Of The Legislation Of The Republic Of Kazakhstan. The Remaining Shelf Life At The Time Of Delivery Must Be At Least 12 Months, Unless A Different Period Is Agreed By The Customer. Terms Of Delivery: Delivery Is Carried Out To The Customer’S Location. The Costs Of Delivery, Loading And Unloading Are Borne By Supplier. The Product Is Supplied In Original Factory Packaging., Aldaron 50 Mg No. 30 With Delivery To The Customer Rk-Ls-5 No. 015623 C03da01, C10aa05 Atorvastatin Film-Coated Tablets, 20 Mg Rk-Ls-5№021218 Delivery To The Customer, Certificate
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