Oxycodone Hydrochloride 68084-0983
Product NDC
68084-0983- Manufacturer
- American Health Packaging
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- February 10, 2020
- Listing Expires
- December 31, 2026
- Application
- ANDA091393
Active Ingredients
| Ingredient | Strength |
|---|---|
| Oxycodone Hydrochloride | 30 mg/1 |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(1)
100 BLISTER PACK in 1 CARTON (68084-983-01) / 1 TABLET in 1 BLISTER PACK (68084-983-11)