Drugplain

NDC 65862-117-01

Benazepril Hydrochloride 20 mg/1

Benazepril Hydrochloride · TABLET, FILM COATED

No Recall History

Benazepril Hydrochloride is a tablet, film coated containing benazepril hydrochloride at a strength of 20 mg/1. Manufactured by Aurobindo Pharma Limited.

Key Facts

Brand Name
Benazepril Hydrochloride
Generic Name
Benazepril Hydrochloride
NDC Code (Package)
65862-117-01
NDC Code (Product)
65862-117
Manufacturer
Aurobindo Pharma Limited
Strength
20 mg/1
Dosage Form
TABLET, FILM COATED
Route
ORAL
Marketing Status
Application #
ANDA078212
Marketing Start
05/22/2008

Recall History

No Recall History

Not medical advice. This information is for reference only. Always consult your doctor or pharmacist.