Oxycodone Hydrochloride 00406-8556
Product NDC
00406-8556- Manufacturer
- Specgx Llc
- Dosage Form
- Solution
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- April 30, 2018
- Listing Expires
- December 31, 2026
- Application
- ANDA210758
Active Ingredients
| Ingredient | Strength |
|---|---|
| Oxycodone Hydrochloride | 5 mg/5mL |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(1)
1 BOTTLE, PLASTIC in 1 CARTON (0406-8556-05) / 500 mL in 1 BOTTLE, PLASTIC