Oxycodone Hydrochloride 72189-0095
Product NDC
72189-0095- Manufacturer
- Direct Rx
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- June 15, 2020
- Listing Expires
- December 31, 2026
- Application
- ANDA204021
Active Ingredients
| Ingredient | Strength |
|---|---|
| Oxycodone Hydrochloride | 5 mg/1 |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(3)
30 TABLET in 1 BOTTLE (72189-095-30)
60 TABLET in 1 BOTTLE (72189-095-60)
90 TABLET in 1 BOTTLE (72189-095-90)