Oxycodone Hydrochloride 76420-0364
Product NDC
76420-0364- Manufacturer
- Asclemed Usa, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- September 10, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA077712
Active Ingredients
| Ingredient | Strength |
|---|---|
| Oxycodone Hydrochloride | 15 mg/1 |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(6)
100 TABLET in 1 BOTTLE, PLASTIC (76420-364-01)
500 TABLET in 1 BOTTLE, PLASTIC (76420-364-05)
10 TABLET in 1 BOTTLE, PLASTIC (76420-364-10)
30 TABLET in 1 BOTTLE, PLASTIC (76420-364-30)
60 TABLET in 1 BOTTLE, PLASTIC (76420-364-60)
90 TABLET in 1 BOTTLE, PLASTIC (76420-364-90)