Oxycodone Hydrochloride 72865-0129
Product NDC
72865-0129- Manufacturer
- Xlcare Pharmaceuticals, Inc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- February 25, 2020
- Listing Expires
- December 31, 2026
- Application
- ANDA207418
Active Ingredients
| Ingredient | Strength |
|---|---|
| Oxycodone Hydrochloride | 30 mg/1 |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(2)
100 TABLET in 1 BOTTLE (72865-129-01)
500 TABLET in 1 BOTTLE (72865-129-05)