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Losartan Potassium and Hydrochlorothiazide - 0603-4229-02 - (Losartan Potassium and Hydrochlorothiazide)

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Drug Information of Losartan Potassium and Hydrochlorothiazide

Product NDC: 0603-4229
Proprietary Name: Losartan Potassium and Hydrochlorothiazide
Non Proprietary Name: Losartan Potassium and Hydrochlorothiazide
Active Ingredient(s): 12.5; 100    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: 0603-4229
Labeler Name: Qualitest Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091617
Marketing Category: ANDA
Start Marketing Date: 20120228

Package Information of Losartan Potassium and Hydrochlorothiazide

Package NDC: 0603-4229-02
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (0603-4229-02)

NDC Information of Losartan Potassium and Hydrochlorothiazide

NDC Code 0603-4229-02
Proprietary Name Losartan Potassium and Hydrochlorothiazide
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (0603-4229-02)
Product NDC 0603-4229
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 20120228
Marketing Category Name ANDA
Labeler Name Qualitest Pharmaceuticals
Substance Name HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM
Strength Number 12.5; 100
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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