Oxycodone Hydrochloride 10702-0023
Product NDC
10702-0023- Manufacturer
- Kvk-Tech, Inc.
- Dosage Form
- Capsule
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- August 20, 2015
- Listing Expires
- December 31, 2026
- Application
- ANDA202773
Active Ingredients
| Ingredient | Strength |
|---|---|
| Oxycodone Hydrochloride | 5 mg/1 |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(2)
100 CAPSULE in 1 BOTTLE (10702-023-01)
60 CAPSULE in 1 BOTTLE (10702-023-06)