Home – Benazepril hydrochloride

Benazepril hydrochloride

FULL PRESCRIBING INFORMATION

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

Benazepril hydrochloride

Benazepril hydrochloride TABLET, FILM COATED

Product Information
Product Type	Human prescription drug label	Item Code (Source)	NDC:51655-067(NDC:63304-339)
Route of Administration	ORAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENAZEPRIL HYDROCHLORIDE BENAZEPRILAT		20 mg

Product Characteristics
Color	Size	Imprint Code	Shape
gray	5 mm	343	ROUND

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	2014-05-30

PLEASE, BE CAREFUL!

Be sure to consult your doctor before taking any medication!