Home > National Drug Code (NDC) > ENALAPRIL MALEATE AND HYDROCHLOROTHIAZIDE

ENALAPRIL MALEATE AND HYDROCHLOROTHIAZIDE - 54868-5503-0 - (ENALAPRIL MALEATE AND HYDROCHLOROTHIAZIDE)

Alphabetical Index


Drug Information of ENALAPRIL MALEATE AND HYDROCHLOROTHIAZIDE

Product NDC: 54868-5503
Proprietary Name: ENALAPRIL MALEATE AND HYDROCHLOROTHIAZIDE
Non Proprietary Name: ENALAPRIL MALEATE AND HYDROCHLOROTHIAZIDE
Active Ingredient(s): 5; 12.5    g/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: 54868-5503
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076486
Marketing Category: ANDA
Start Marketing Date: 20060110

Package Information of ENALAPRIL MALEATE AND HYDROCHLOROTHIAZIDE

Package NDC: 54868-5503-0
Package Description: 30 TABLET in 1 BOTTLE (54868-5503-0)

NDC Information of ENALAPRIL MALEATE AND HYDROCHLOROTHIAZIDE

NDC Code 54868-5503-0
Proprietary Name ENALAPRIL MALEATE AND HYDROCHLOROTHIAZIDE
Package Description 30 TABLET in 1 BOTTLE (54868-5503-0)
Product NDC 54868-5503
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ENALAPRIL MALEATE AND HYDROCHLOROTHIAZIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20060110
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name ENALAPRIL MALEATE; HYDROCHLOROTHIAZIDE
Strength Number 5; 12.5
Strength Unit g/1; mg/1
Pharmaceutical Classes Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]

Complete Information of ENALAPRIL MALEATE AND HYDROCHLOROTHIAZIDE


General Information