Oxycodone Hcl 72189-0632
Product NDC
72189-0632- Manufacturer
- Direct_rx
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- July 22, 2025
- Listing Expires
- December 31, 2026
- Application
- ANDA077712
Active Ingredients
| Ingredient | Strength |
|---|---|
| Oxycodone Hydrochloride | 10 mg/1 |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(3)
30 TABLET in 1 BOTTLE (72189-632-30)
60 TABLET in 1 BOTTLE (72189-632-60)
90 TABLET in 1 BOTTLE (72189-632-90)