Lotensin - 0078-0450-05 - (Benazepril Hydrochloride)

Alphabetical Index


Drug Information of Lotensin

Product NDC: 0078-0450
Proprietary Name: Lotensin
Non Proprietary Name: Benazepril Hydrochloride
Active Ingredient(s): 40    mg/1 & nbsp;   Benazepril Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Lotensin

Product NDC: 0078-0450
Labeler Name: Novartis Pharmaceuticals Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019851
Marketing Category: NDA
Start Marketing Date: 19910625

Package Information of Lotensin

Package NDC: 0078-0450-05
Package Description: 100 TABLET in 1 BOTTLE (0078-0450-05)

NDC Information of Lotensin

NDC Code 0078-0450-05
Proprietary Name Lotensin
Package Description 100 TABLET in 1 BOTTLE (0078-0450-05)
Product NDC 0078-0450
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Benazepril Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19910625
Marketing Category Name NDA
Labeler Name Novartis Pharmaceuticals Corporation
Substance Name BENAZEPRIL HYDROCHLORIDE
Strength Number 40
Strength Unit mg/1
Pharmaceutical Classes Angiontensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE]

Complete Information of Lotensin


General Information