Oxycodone Hydrochloride 00115-1560
Product NDC
00115-1560- Manufacturer
- Amneal Pharmaceuticals Of New York Llc
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- February 22, 2016
- Listing Expires
- December 31, 2027
- Application
- NDA022272
Active Ingredients
| Ingredient | Strength |
|---|---|
| Oxycodone Hydrochloride | 40 mg/1 |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(1)
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0115-1560-01)