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Losartan Potassium and Hydrochlorothiazide - 52125-397-19 - (Losartan Potassium and Hydrochlorothiazide)

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Drug Information of Losartan Potassium and Hydrochlorothiazide

Product NDC: 52125-397
Proprietary Name: Losartan Potassium and Hydrochlorothiazide
Non Proprietary Name: Losartan Potassium and Hydrochlorothiazide
Active Ingredient(s): 12.5    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: 52125-397
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090528
Marketing Category: ANDA
Start Marketing Date: 20130209

Package Information of Losartan Potassium and Hydrochlorothiazide

Package NDC: 52125-397-19
Package Description: 90 TABLET in 1 VIAL (52125-397-19)

NDC Information of Losartan Potassium and Hydrochlorothiazide

NDC Code 52125-397-19
Proprietary Name Losartan Potassium and Hydrochlorothiazide
Package Description 90 TABLET in 1 VIAL (52125-397-19)
Product NDC 52125-397
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Losartan Potassium and Hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130209
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name HYDROCHLOROTHIAZIDE
Strength Number 12.5
Strength Unit mg/1
Pharmaceutical Classes Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]

Complete Information of Losartan Potassium and Hydrochlorothiazide


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