Oxycodone Hydrochloride 68071-2899
Product NDC
68071-2899- Manufacturer
- Nucare Pharmaceuticals,inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- September 8, 2014
- Listing Expires
- December 31, 2026
- Application
- ANDA091490
Active Ingredients
| Ingredient | Strength |
|---|---|
| Oxycodone Hydrochloride | 5 mg/1 |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(2)
4 TABLET in 1 BOTTLE, PLASTIC (68071-2899-4)
6 TABLET in 1 BOTTLE, PLASTIC (68071-2899-6)