Label: BENAZEPRIL HYDROCHLORIDE tablet, film coated
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Contains inactivated NDC Code(s)
NDC Code(s): 51655-067-52 - Packager: Northwind Pharmaceuticals
- This is a repackaged label.
- Source NDC Code(s): 63304-339
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated June 2, 2014
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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
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INGREDIENTS AND APPEARANCE
BENAZEPRIL HYDROCHLORIDE
benazepril hydrochloride tablet, film coatedProduct 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)