NDC 62559-414-01
Benazepril Hydrochloride and Hydrochlorothiazide 5 mg/1
Benazepril Hydrochloride and Hydrochlorothiazide · TABLET
Benazepril Hydrochloride and Hydrochlorothiazide is a tablet containing benazepril hydrochloride and hydrochlorothiazide at a strength of 5 mg/1. Manufactured by ANI Pharmaceuticals, Inc..
Key Facts
- Brand Name
- Benazepril Hydrochloride and Hydrochlorothiazide
- Generic Name
- Benazepril Hydrochloride and Hydrochlorothiazide
- NDC Code (Package)
62559-414-01- NDC Code (Product)
62559-414- Manufacturer
- ANI Pharmaceuticals, Inc.
- Strength
- 5 mg/1
- Dosage Form
- TABLET
- Route
- ORAL
- Marketing Status
- Application #
- ANDA076342
- Drug Class
- Thiazide Diuretic [EPC]
- Marketing Start
- 11/07/2022
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.