NDC 68462-209-90
Moexipril Hydrochloride 7.5 mg/1
Moexipril Hydrochloride · TABLET, FILM COATED
Moexipril Hydrochloride is a tablet, film coated containing moexipril hydrochloride at a strength of 7.5 mg/1. Manufactured by Glenmark Pharmaceuticals Inc., USA.
Key Facts
- Brand Name
- Moexipril Hydrochloride
- Generic Name
- Moexipril Hydrochloride
- NDC Code (Package)
68462-209-90- NDC Code (Product)
68462-209- Manufacturer
- Glenmark Pharmaceuticals Inc., USA
- Strength
- 7.5 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- ANDA090416
- Marketing Start
- 12/31/2010
Recall History
No Recall HistoryView Full Drug Page
Moexipril Hydrochloride — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.