NDC 49884-117-01
Amiloride Hydrochloride 5 mg/1
Amiloride Hydrochloride · TABLET
Amiloride Hydrochloride is a tablet containing amiloride hydrochloride at a strength of 5 mg/1. Manufactured by Endo USA, Inc..
Key Facts
- Brand Name
- Amiloride Hydrochloride
- Generic Name
- Amiloride Hydrochloride
- NDC Code (Package)
49884-117-01- NDC Code (Product)
49884-117- Manufacturer
- Endo USA, Inc.
- Strength
- 5 mg/1
- Dosage Form
- TABLET
- Route
- ORAL
- Marketing Status
- Application #
- ANDA070346
- Marketing Start
- 01/22/1986
Recall History
No Recall HistoryView Full Drug Page
Amiloride Hydrochloride — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.