NDC 51655-388-52
Benazepril Hydrochloride 20 mg/1
Benazepril Hydrochloride · TABLET, FILM COATED
Benazepril Hydrochloride is a tablet, film coated containing benazepril hydrochloride at a strength of 20 mg/1. Manufactured by Northwind Health Company, LLC.
Key Facts
- Brand Name
- Benazepril Hydrochloride
- Generic Name
- Benazepril Hydrochloride
- NDC Code (Package)
51655-388-52- NDC Code (Product)
51655-388- Manufacturer
- Northwind Health Company, LLC
- Strength
- 20 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- ANDA078212
- Marketing Start
- 05/19/2023
Recall History
No Recall HistoryView Full Drug Page
Benazepril Hydrochloride — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.