NDC 30698-449-01
Lotensin 20 mg/1
benazepril hydrochloride · TABLET
Lotensin is a tablet containing benazepril hydrochloride at a strength of 20 mg/1. Manufactured by Validus Pharmaceuticals LLC.
Key Facts
- Brand Name
- Lotensin
- Generic Name
- benazepril hydrochloride
- NDC Code (Package)
30698-449-01- NDC Code (Product)
30698-449- Manufacturer
- Validus Pharmaceuticals LLC
- Strength
- 20 mg/1
- Dosage Form
- TABLET
- Route
- ORAL
- Marketing Status
- Application #
- NDA019851
- Marketing Start
- 06/21/1991
Recall History
No Recall HistoryView Full Drug Page
Lotensin — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.