Oxycodone Hydrochloride 10702-0171
Product NDC
10702-0171- Manufacturer
- Kvk-Tech, Inc.
- Dosage Form
- Solution
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- July 21, 2017
- Listing Expires
- December 31, 2026
- Application
- ANDA208593
Active Ingredients
| Ingredient | Strength |
|---|---|
| Oxycodone Hydrochloride | 100 mg/5mL |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(1)
1 BOTTLE, PLASTIC in 1 CARTON (10702-171-03) / 30 mL in 1 BOTTLE, PLASTIC