Oxycodone Hydrochloride 68071-2368
Product NDC
68071-2368- Manufacturer
- Nucare Pharmaceuticals,inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- July 12, 2012
- Listing Expires
- December 31, 2027
- Application
- ANDA202160
Active Ingredients
| Ingredient | Strength |
|---|---|
| Oxycodone Hydrochloride | 5 mg/1 |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(1)
6 TABLET in 1 BOTTLE (68071-2368-6)