Oxycodone Hydrochloride 10702-0018
Product NDC
10702-0018- Manufacturer
- Kvk-Tech,inc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- October 18, 2013
- Listing Expires
- December 31, 2027
- Application
- ANDA091393
Active Ingredients
| Ingredient | Strength |
|---|---|
| Oxycodone Hydrochloride | 5 mg/1 |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(2)
100 TABLET in 1 BOTTLE (10702-018-01)
500 TABLET in 1 BOTTLE (10702-018-50)