Oxycodone Hydrochloride 43386-0434
Product NDC
43386-0434- Manufacturer
- Lupin Pharmaceuticals,inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- June 12, 2017
- Listing Expires
- December 31, 2026
- Application
- ANDA204021
Active Ingredients
| Ingredient | Strength |
|---|---|
| Oxycodone Hydrochloride | 20 mg/1 |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(1)
100 TABLET in 1 BOTTLE (43386-434-01)