NDC 0574-0229-01
benazepril hydrochloride and hydrochlorothiazide 20 mg/1
benazepril hydrochloride and hydrochlorothiazide · TABLET
benazepril hydrochloride and hydrochlorothiazide is a tablet containing benazepril hydrochloride and hydrochlorothiazide at a strength of 20 mg/1. Manufactured by Padagis US LLC.
Key Facts
- Brand Name
- benazepril hydrochloride and hydrochlorothiazide
- Generic Name
- benazepril hydrochloride and hydrochlorothiazide
- NDC Code (Package)
0574-0229-01- NDC Code (Product)
0574-0229- Manufacturer
- Padagis US LLC
- 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 HistoryView Full Drug Page
benazepril hydrochloride and hydrochlorothiazide — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.