Oxycodone And Acetaminophen 72887-0682
Product NDC
72887-0682- Manufacturer
- Fh2 Pharma Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- March 2, 2021
- Listing Expires
- December 31, 2027
- Application
- ANDA040608
Active Ingredients
| Ingredient | Strength |
|---|---|
| Acetaminophen | 300 mg/1 |
| Oxycodone Hydrochloride | 7.5 mg/1 |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(1)
30 TABLET in 1 BOTTLE (72887-682-03)