Home > National Drug Code (NDC) > Enalapril Maleate and Hydrochlorothiazide

Enalapril Maleate and Hydrochlorothiazide - 0378-0723-01 - (enalapril maleate and hydrochlorothiazide)

Alphabetical Index


Drug Information of Enalapril Maleate and Hydrochlorothiazide

Product NDC: 0378-0723
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: 0378-0723
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075624
Marketing Category: ANDA
Start Marketing Date: 20121009

Package Information of Enalapril Maleate and Hydrochlorothiazide

Package NDC: 0378-0723-01
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (0378-0723-01)

NDC Information of Enalapril Maleate and Hydrochlorothiazide

NDC Code 0378-0723-01
Proprietary Name Enalapril Maleate and Hydrochlorothiazide
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (0378-0723-01)
Product NDC 0378-0723
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name enalapril maleate and hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20121009
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals Inc.
Substance Name ENALAPRIL MALEATE; HYDROCHLOROTHIAZIDE
Strength Number 10; 25
Strength Unit mg/1; mg/1
Pharmaceutical Classes Angiontensin 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