Oxycodone Hydrochloride And Acetaminophen 64850-0622
Product NDC
64850-0622- Manufacturer
- Elite Laboratories, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- December 4, 2017
- Listing Expires
- December 31, 2027
- Application
- ANDA209385
Active Ingredients
| Ingredient | Strength |
|---|---|
| Acetaminophen | 325 mg/1 |
| Oxycodone Hydrochloride | 7.5 mg/1 |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(2)
100 TABLET in 1 BOTTLE (64850-622-01)
500 TABLET in 1 BOTTLE (64850-622-05)