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LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE - 65841-732-06 - (LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE)

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Drug Information of LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE

Product NDC: 65841-732
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: 65841-732
Labeler Name: Cadila Healthcare Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078385
Marketing Category: ANDA
Start Marketing Date: 20100410

Package Information of LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE

Package NDC: 65841-732-06
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (65841-732-06)

NDC Information of LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE

NDC Code 65841-732-06
Proprietary Name LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (65841-732-06)
Product NDC 65841-732
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 20100410
Marketing Category Name ANDA
Labeler Name Cadila Healthcare Limited
Substance Name HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM
Strength Number 12.5; 50
Strength Unit mg/1; mg/1
Pharmaceutical Classes Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient],Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]

Complete Information of LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE


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