Univasc - 0091-3707-01 - (moexipril hydrochloride)

Alphabetical Index


Drug Information of Univasc

Product NDC: 0091-3707
Proprietary Name: Univasc
Non Proprietary Name: moexipril hydrochloride
Active Ingredient(s): 7.5    mg/1 & nbsp;   moexipril hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Univasc

Product NDC: 0091-3707
Labeler Name: UCB, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020312
Marketing Category: NDA
Start Marketing Date: 19950715

Package Information of Univasc

Package NDC: 0091-3707-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (0091-3707-01)

NDC Information of Univasc

NDC Code 0091-3707-01
Proprietary Name Univasc
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (0091-3707-01)
Product NDC 0091-3707
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name moexipril hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19950715
Marketing Category Name NDA
Labeler Name UCB, Inc.
Substance Name MOEXIPRIL HYDROCHLORIDE
Strength Number 7.5
Strength Unit mg/1
Pharmaceutical Classes Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]

Complete Information of Univasc


General Information