BENAZEPRIL HYDROCHLORIDE powder

Benazepril Hydrochloride by

Drug Labeling and Warnings

Benazepril Hydrochloride by is a Other medication manufactured, distributed, or labeled by H3 MEDICAL INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Principle Display Panel

INGREDIENTS AND APPEARANCE

BENAZEPRIL HYDROCHLORIDE 
benazepril hydrochloride powder

Product Information
Product Type	BULK INGREDIENT	Item Code (Source)	NDC: 63732-2002
Route of Administration	NOT APPLICABLE

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENAZEPRIL HYDROCHLORIDE (UNII: N1SN99T69T) (BENAZEPRILAT - UNII:JRM708L703)	BENAZEPRIL HYDROCHLORIDE	1 g  in 1 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63732-2002-4	100 g in 1 BOTTLE	12/01/2014
2	NDC: 63732-2002-5	500 g in 1 BOTTLE	12/01/2014
3	NDC: 63732-2002-6	1000 g in 1 BOTTLE	12/01/2014

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
bulk ingredient for animal drug compounding		12/01/2014

Labeler - H3 MEDICAL INC. (202872487)

Establishment
Name	Address	ID/FEI	Business Operations
H3 MEDICAL INC.		202872487	relabel(63732-2002)