Oxycodone Hydrochloride 00406-0552
Product NDC
00406-0552- Manufacturer
- Specgx Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- June 30, 2004
- Listing Expires
- December 31, 2027
- Application
- ANDA076758
Active Ingredients
| Ingredient | Strength |
|---|---|
| Oxycodone Hydrochloride | 5 mg/1 |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(3)
100 TABLET in 1 BOTTLE (0406-0552-01)
1 TABLET in 1 BLISTER PACK (0406-0552-23)
100 TABLET in 1 BLISTER PACK (0406-0552-62)