Drugplain

NDC 72162-2328-1

benazepril hydrochloride and hydrochlorothiazide 20 mg/1

benazepril hydrochloride and hydrochlorothiazide · TABLET

No Recall History

benazepril hydrochloride and hydrochlorothiazide is a tablet containing benazepril hydrochloride and hydrochlorothiazide at a strength of 20 mg/1. Manufactured by Bryant Ranch Prepack.

Key Facts

Brand Name
benazepril hydrochloride and hydrochlorothiazide
Generic Name
benazepril hydrochloride and hydrochlorothiazide
NDC Code (Package)
72162-2328-1
NDC Code (Product)
72162-2328
Manufacturer
Bryant Ranch Prepack
Strength
20 mg/1
Dosage Form
TABLET
Route
ORAL
Marketing Status
Application #
NDA020033
Drug Class
Thiazide Diuretic [EPC]
Marketing Start
04/07/2019

Recall History

No Recall History

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