Oxycodone Hydrochloride 31722-0485
Product NDC
31722-0485- Manufacturer
- Camber Pharmaceuticals Inc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- November 14, 2025
- Listing Expires
- December 31, 2027
- Application
- ANDA207418
Active Ingredients
| Ingredient | Strength |
|---|---|
| Oxycodone Hydrochloride | 10 mg/1 |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(2)
100 TABLET in 1 BOTTLE (31722-485-01)
500 TABLET in 1 BOTTLE (31722-485-05)