Oxycodone Hydrochloride 43386-0920
Product NDC
43386-0920- Manufacturer
- Lupin Pharmaceuticals, Inc.
- Dosage Form
- Solution
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- April 29, 2015
- Listing Expires
- December 31, 2026
- Application
- ANDA204603
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 (43386-920-60) / 30 mL in 1 BOTTLE