NDC 64896-697-03
Oxymorphone hydrochloride 10 mg/1
Oxymorphone hydrochloride · TABLET, FILM COATED, EXTENDED RELEASE
Oxymorphone hydrochloride is a tablet, film coated, extended release containing oxymorphone hydrochloride at a strength of 10 mg/1. Manufactured by Amneal Pharmaceuticals LLC.
Key Facts
- Brand Name
- Oxymorphone hydrochloride
- Generic Name
- Oxymorphone hydrochloride
- NDC Code (Package)
64896-697-03- NDC Code (Product)
64896-697- Manufacturer
- Amneal Pharmaceuticals LLC
- Strength
- 10 mg/1
- Dosage Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- DEA Schedule
- Schedule II (Controlled)
- Application #
- ANDA079087
- Marketing Start
- 01/02/2013
Recall History
No Recall HistoryView Full Drug Page
Oxymorphone hydrochloride — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.