NDC 68462-579-01
Benazepril Hydrochloride and Hydrochlorothiazide 20 mg/1
Benazepril Hydrochloride and Hydrochlorothiazide · TABLET, FILM COATED
Benazepril Hydrochloride and Hydrochlorothiazide is a tablet, film coated containing benazepril hydrochloride and hydrochlorothiazide at a strength of 20 mg/1. Manufactured by Glenmark Pharmaceuticals Inc., USA.
Key Facts
- Brand Name
- Benazepril Hydrochloride and Hydrochlorothiazide
- Generic Name
- Benazepril Hydrochloride and Hydrochlorothiazide
- NDC Code (Package)
68462-579-01- NDC Code (Product)
68462-579- Manufacturer
- Glenmark Pharmaceuticals Inc., USA
- Strength
- 20 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- ANDA076631
- Drug Class
- Thiazide Diuretic [EPC]
- Marketing Start
- 02/11/2004
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.