Oxycodone And Acetaminophen 61919-0871
Product NDC
61919-0871- Manufacturer
- Direct_rx
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- August 21, 2019
- Listing Expires
- December 31, 2026
- Application
- ANDA207419
Active Ingredients
| Ingredient | Strength |
|---|---|
| Acetaminophen | 325 mg/1 |
| Oxycodone Hydrochloride | 10 mg/1 |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(2)
60 TABLET in 1 BOTTLE (61919-871-60)
120 TABLET in 1 BOTTLE (61919-871-72)