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Enalapril Maleate and Hydrochlorothiazide - 51672-4046-3 - (Enalapril Maleate and Hydrochlorothiazide)

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Drug Information of Enalapril Maleate and Hydrochlorothiazide

Product NDC: 51672-4046
Proprietary Name: Enalapril Maleate and Hydrochlorothiazide
Non Proprietary Name: Enalapril Maleate and Hydrochlorothiazide
Active Ingredient(s): 10; 25    mg/1; mg/1 & nbsp;   Enalapril Maleate and Hydrochlorothiazide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Enalapril Maleate and Hydrochlorothiazide

Product NDC: 51672-4046
Labeler Name: Taro Pharmaceuticals U.S.A., Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075788
Marketing Category: ANDA
Start Marketing Date: 20010918

Package Information of Enalapril Maleate and Hydrochlorothiazide

Package NDC: 51672-4046-3
Package Description: 1000 TABLET in 1 BOTTLE (51672-4046-3)

NDC Information of Enalapril Maleate and Hydrochlorothiazide

NDC Code 51672-4046-3
Proprietary Name Enalapril Maleate and Hydrochlorothiazide
Package Description 1000 TABLET in 1 BOTTLE (51672-4046-3)
Product NDC 51672-4046
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Enalapril Maleate and Hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20010918
Marketing Category Name ANDA
Labeler Name Taro Pharmaceuticals U.S.A., Inc.
Substance Name ENALAPRIL MALEATE; HYDROCHLOROTHIAZIDE
Strength Number 10; 25
Strength Unit mg/1; mg/1
Pharmaceutical Classes Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]

Complete Information of Enalapril Maleate and Hydrochlorothiazide


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