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Losartan Potassium and Hydrochlorothiazide - 60505-2917-0 - (Losartan Potassium and Hydrochlorothiazide)

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Drug Information of Losartan Potassium and Hydrochlorothiazide

Product NDC: 60505-2917
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, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Losartan Potassium and Hydrochlorothiazide

Product NDC: 60505-2917
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090150
Marketing Category: ANDA
Start Marketing Date: 20101006

Package Information of Losartan Potassium and Hydrochlorothiazide

Package NDC: 60505-2917-0
Package Description: 10 BLISTER PACK in 1 CARTON (60505-2917-0) > 10 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Losartan Potassium and Hydrochlorothiazide

NDC Code 60505-2917-0
Proprietary Name Losartan Potassium and Hydrochlorothiazide
Package Description 10 BLISTER PACK in 1 CARTON (60505-2917-0) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 60505-2917
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 20101006
Marketing Category Name ANDA
Labeler Name Apotex Corp.
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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