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Losartan Potassium and Hydrochlorothiazide - 13668-118-74 - (Losartan Potassium and Hydrochlorothiazide)

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Drug Information of Losartan Potassium and Hydrochlorothiazide

Product NDC: 13668-118
Proprietary Name: Losartan Potassium and Hydrochlorothiazide
Non Proprietary Name: Losartan Potassium and Hydrochlorothiazide
Active Ingredient(s): 25; 100    mg/1; mg/1 & nbsp;   Losartan Potassium and Hydrochlorothiazide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Losartan Potassium and Hydrochlorothiazide

Product NDC: 13668-118
Labeler Name: Torrent Pharmaceuticals Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090528
Marketing Category: ANDA
Start Marketing Date: 20101006

Package Information of Losartan Potassium and Hydrochlorothiazide

Package NDC: 13668-118-74
Package Description: 100 TABLET in 1 CARTON (13668-118-74)

NDC Information of Losartan Potassium and Hydrochlorothiazide

NDC Code 13668-118-74
Proprietary Name Losartan Potassium and Hydrochlorothiazide
Package Description 100 TABLET in 1 CARTON (13668-118-74)
Product NDC 13668-118
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Losartan Potassium and Hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101006
Marketing Category Name ANDA
Labeler Name Torrent Pharmaceuticals Limited
Substance Name HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM
Strength Number 25; 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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