Oxycodone Hydrochloride 76420-0761
Product NDC
76420-0761- Manufacturer
- Asclemed Usa, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- September 8, 2014
- Listing Expires
- December 31, 2026
- Application
- ANDA091490
Active Ingredients
| Ingredient | Strength |
|---|---|
| Oxycodone Hydrochloride | 20 mg/1 |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(6)
100 TABLET in 1 BOTTLE, PLASTIC (76420-761-01)
10 TABLET in 1 BOTTLE, PLASTIC (76420-761-10)
20 TABLET in 1 BOTTLE, PLASTIC (76420-761-20)
30 TABLET in 1 BOTTLE, PLASTIC (76420-761-30)
60 TABLET in 1 BOTTLE, PLASTIC (76420-761-60)
90 TABLET in 1 BOTTLE, PLASTIC (76420-761-90)