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Losartan Potassium and Hydrochlorothiazide - 0093-7367-10 - (Losartan Potassium and Hydrochlorothiazide)

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Drug Information of Losartan Potassium and Hydrochlorothiazide

Product NDC: 0093-7367
Proprietary Name: Losartan Potassium and Hydrochlorothiazide
Non Proprietary Name: Losartan Potassium and Hydrochlorothiazide
Active Ingredient(s): 12.5; 50    mg/1; mg/1 & nbsp;   Losartan Potassium and Hydrochlorothiazide
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Losartan Potassium and Hydrochlorothiazide

Product NDC: 0093-7367
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077157
Marketing Category: ANDA
Start Marketing Date: 20100406

Package Information of Losartan Potassium and Hydrochlorothiazide

Package NDC: 0093-7367-10
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (0093-7367-10)

NDC Information of Losartan Potassium and Hydrochlorothiazide

NDC Code 0093-7367-10
Proprietary Name Losartan Potassium and Hydrochlorothiazide
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (0093-7367-10)
Product NDC 0093-7367
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Losartan Potassium and Hydrochlorothiazide
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100406
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM
Strength Number 12.5; 50
Strength Unit mg/1; mg/1
Pharmaceutical Classes Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]

Complete Information of Losartan Potassium and Hydrochlorothiazide


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