Oxycodone Hydrochloride 43602-0190
Product NDC
43602-0190- Manufacturer
- Ascent Pharmaceuticals Inc
- Dosage Form
- Solution
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- July 13, 2017
- Listing Expires
- December 31, 2026
- Application
- ANDA209021
Active Ingredients
| Ingredient | Strength |
|---|---|
| Oxycodone Hydrochloride | 5 mg/5mL |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(2)
30 mL in 1 BOTTLE (43602-190-31)
500 mL in 1 BOTTLE (43602-190-50)