Benazepril Hydrochloride

BENAZEPRIL HYDROCHLORIDE- benazepril hydrochloride tablet, film coated
Northwind Pharmaceuticals

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 HCL 51655-067
(click image for full-size original)

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 DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BENAZEPRIL HYDROCHLORIDE (BENAZEPRILAT) 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 Multilevel Packaging
1 NDC:51655-067-52 30 TABLET, FILM COATED in 1 BOTTLE, DISPENSING None
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 Operations
Northwind Pharmaceuticals 036986393 repack (51655-067)

Revised: 06/2014 Northwind Pharmaceuticals

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