Oxycodone Hydrochloride 71930-0022
Product NDC
71930-0022- Manufacturer
- Eywa Pharma Inc
- Dosage Form
- Solution
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- March 1, 2019
- Listing Expires
- December 31, 2027
- Application
- ANDA207511
Active Ingredients
| Ingredient | Strength |
|---|---|
| Oxycodone Hydrochloride | 5 mg/5mL |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(1)
1 BOTTLE in 1 CARTON (71930-022-43) / 473 mL in 1 BOTTLE