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Losartan Potassium and Hydrochlorothiazide - 13668-116-90 - (Losartan Potassium and Hydrochlorothiazide)

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Drug Information of Losartan Potassium and Hydrochlorothiazide

Product NDC: 13668-116
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
Coding System: National Drug Codes(NDC)

Labeler Information of Losartan Potassium and Hydrochlorothiazide

Product NDC: 13668-116
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: 13668-116-90
Package Description: 90 TABLET in 1 BOTTLE (13668-116-90)

NDC Information of Losartan Potassium and Hydrochlorothiazide

NDC Code 13668-116-90
Proprietary Name Losartan Potassium and Hydrochlorothiazide
Package Description 90 TABLET in 1 BOTTLE (13668-116-90)
Product NDC 13668-116
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 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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