Upgrade to enjoy subscriber-only features like email alerts and data export. See the Plans and Pricing

Serving leading biopharmaceutical companies globally:

Novartis
Citi
Dow
Colorcon
Argus Health
McKinsey
Cantor Fitzgerald
Federal Trade Commission
Chubb
Boehringer Ingelheim

Generated: December 10, 2017

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 076211

« Back to Dashboard

NDA 076211 describes BENAZEPRIL HYDROCHLORIDE, which is a drug marketed by Actavis Labs Fl Inc, Amneal Pharms, Apotex Inc, Aurobindo Pharma, Genpharm, Ivax Sub Teva Pharms, Mylan, Prinston Inc, Sandoz, Sun Pharm Inds Ltd, Teva, Zydus Pharms Usa, and Mylan Pharms Inc, and is included in nineteen NDAs. It is available from forty-three suppliers. Additional details are available on the BENAZEPRIL HYDROCHLORIDE profile page.

The generic ingredient in BENAZEPRIL HYDROCHLORIDE is benazepril hydrochloride; hydrochlorothiazide. There are fourteen drug master file entries for this compound. Twelve suppliers are listed for this compound. Additional details are available on the benazepril hydrochloride; hydrochlorothiazide profile page.

Summary for 076211

Tradename:1
Applicant:1
Ingredient:1
Patents:0
Therapeutic Class:Cardiovascular Agents
Formulation / Manufacturing:see details

Pharmacology for NDA: 076211

Suppliers and Packaging for NDA: 076211

Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
BENAZEPRIL HYDROCHLORIDE benazepril hydrochloride TABLET;ORAL 076211 ANDA Teva Pharmaceuticals USA, Inc. 0093-5124 0093-5124-01 100 TABLET, COATED in 1 BOTTLE (0093-5124-01)
BENAZEPRIL HYDROCHLORIDE benazepril hydrochloride TABLET;ORAL 076211 ANDA Teva Pharmaceuticals USA, Inc. 0093-5125 0093-5125-01 100 TABLET, COATED in 1 BOTTLE (0093-5125-01)

Summary for product number 001

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength5MG
Approval Date:Feb 11, 2004TE:ABRLD:No

Summary for product number 002

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength10MG
Approval Date:Feb 11, 2004TE:ABRLD:No

Summary for product number 003

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength20MG
Approval Date:Feb 11, 2004TE:ABRLD:No


Complete Access Available with Subscription
« Back to Dashboard

For more information try a trial or see the database preview and plans and pricing

Serving leading biopharmaceutical companies globally:

Fish and Richardson
Chubb
Covington
UBS
Teva
Dow
Medtronic
Julphar
Cipla
Argus Health

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. thinkBiotech performs no independent verifification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.

Copyright 2002-2017 thinkBiotech LLC
ISSN: 2162-2639

Secure SSL Encrypted
Privacy and Cookies
Terms & Conditions

Follow DrugPatentWatch:

botpot