Oxycodone Hydrochloride 71930-0023
Product NDC
71930-0023- Manufacturer
- Eywa Pharma Inc
- Dosage Form
- Solution
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- June 1, 2018
- Listing Expires
- December 31, 2027
- Application
- ANDA209897
Active Ingredients
| Ingredient | Strength |
|---|---|
| Oxycodone Hydrochloride | 20 mg/mL |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(1)
1 BOTTLE in 1 CARTON (71930-023-30) / 30 mL in 1 BOTTLE