Oxycodone Hydrochloride 13107-0056
Product NDC
13107-0056- Manufacturer
- Aurolife Pharma, Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- July 12, 2012
- Listing Expires
- December 31, 2026
- Application
- ANDA202160
Active Ingredients
| Ingredient | Strength |
|---|---|
| Oxycodone Hydrochloride | 15 mg/1 |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(3)
100 TABLET in 1 BOTTLE (13107-056-01)
30 TABLET in 1 BOTTLE (13107-056-30)
1000 TABLET in 1 BOTTLE (13107-056-99)