Oxymorphone Hydrochloride 31722-0929
Product NDC
31722-0929- Manufacturer
- Camber Pharmaceuticals, Inc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- March 1, 2018
- Listing Expires
- December 31, 2026
- Application
- ANDA210175
Active Ingredients
| Ingredient | Strength |
|---|---|
| Oxymorphone Hydrochloride | 5 mg/1 |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(1)
100 TABLET in 1 BOTTLE (31722-929-01)