Oxycodone Hcl 72189-0611
Product NDC
72189-0611- Manufacturer
- Direct_rx
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- March 24, 2025
- Listing Expires
- December 31, 2026
- Application
- ANDA091393
Active Ingredients
| Ingredient | Strength |
|---|---|
| Oxycodone Hydrochloride | 5 mg/1 |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(1)
30 TABLET in 1 BOTTLE (72189-611-30)