BENAZEPRIL HYDROCHLORIDE tablet, film coated

Benazepril hydrochloride by

Drug Labeling and Warnings

Benazepril hydrochloride by is a Prescription medication manufactured, distributed, or labeled by Northwind Pharmaceuticals. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PRINCIPAL DISPLAY PANEL

NDC: 51655-067-52

MFG: 63304-0339-05

Benazepril Hydrochloride 20 MG

30 Tablets

Rx only

Lot# NW89620001

Exp Date: 2/2015

Each tablet contains: Benasepril hydrochloride, USP....20 MG

Dosage: See package outsert for full prescribing information

Store at 60 to 77 degrees F.

Store in a tight, light-resistanct container.  Keep this and all medications out the the reach of children.

Mfg by: Zhejiang Huahai Pharm. Co., Ltd Linhai, Zheijang, China for Ranbaxy Pharmaceuticals Inc, Jacksonville, FL 32257 USA

lot # 316B13002 Exp 2/2015

Repackaged by Northwind Pharmaceuticals, Indianapolis, IN 46256

WARNINGS AND PRECAUTIONS

INGREDIENTS AND APPEARANCE

BENAZEPRIL HYDROCHLORIDE 
benazepril hydrochloride tablet, film coated

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 51655-067(NDC:63304-339)
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENAZEPRIL HYDROCHLORIDE (UNII: N1SN99T69T) (BENAZEPRILAT - UNII:JRM708L703)	BENAZEPRIL HYDROCHLORIDE	20 mg

Product Characteristics
Color	gray	Score	no score
Shape	ROUND	Size	5mm
Flavor		Imprint Code	343
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51655-067-52	30 in 1 BOTTLE, DISPENSING

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
ANDA	ANDA076118	05/30/2014

Labeler - Northwind Pharmaceuticals (036986393)

Registrant - Northwind Pharmaceuticals (036986393)

Establishment
Name	Address	ID/FEI	Business Operations
Northwind Pharmaceuticals		036986393	repack(51655-067)