Lotensin - 54868-2350-2 - (Benazepril Hydrochloride)

Alphabetical Index


Drug Information of Lotensin

Product NDC: 54868-2350
Proprietary Name: Lotensin
Non Proprietary Name: Benazepril Hydrochloride
Active Ingredient(s): 10    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: 54868-2350
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019851
Marketing Category: NDA
Start Marketing Date: 20031104

Package Information of Lotensin

Package NDC: 54868-2350-2
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (54868-2350-2)

NDC Information of Lotensin

NDC Code 54868-2350-2
Proprietary Name Lotensin
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (54868-2350-2)
Product NDC 54868-2350
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Benazepril Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20031104
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name BENAZEPRIL HYDROCHLORIDE
Strength Number 10
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