Home > National Drug Code (NDC) > Moexipril Hydrochloride

Moexipril Hydrochloride - 68462-208-10 - (Moexipril Hydrochloride)

Alphabetical Index


Drug Information of Moexipril Hydrochloride

Product NDC: 68462-208
Proprietary Name: Moexipril Hydrochloride
Non Proprietary Name: Moexipril Hydrochloride
Active Ingredient(s): 15    mg/1 & nbsp;   Moexipril Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Moexipril Hydrochloride

Product NDC: 68462-208
Labeler Name: Glenmark Generics Inc., USA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090416
Marketing Category: ANDA
Start Marketing Date: 20101231

Package Information of Moexipril Hydrochloride

Package NDC: 68462-208-10
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (68462-208-10)

NDC Information of Moexipril Hydrochloride

NDC Code 68462-208-10
Proprietary Name Moexipril Hydrochloride
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (68462-208-10)
Product NDC 68462-208
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Moexipril Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20101231
Marketing Category Name ANDA
Labeler Name Glenmark Generics Inc., USA
Substance Name MOEXIPRIL HYDROCHLORIDE
Strength Number 15
Strength Unit mg/1
Pharmaceutical Classes Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]

Complete Information of Moexipril Hydrochloride


General Information