NDC 10702-057 – Oxycodone Hydrochloride
Oxycodone Hydrochloride 20 mg/1 · Tablet · Oral
Product NDC10702-057
Product details
- Brand name
- Oxycodone Hydrochloride
- Generic name
- Oxycodone Hydrochloride
- Labeler
- KVK-TECH,INC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA091393
- Marketed since
- October 18, 2013
- Listing expires
- December 31, 2027
- Pharmacologic class
- Opioid Agonist
Active ingredients
- Oxycodone Hydrochloride 20 mg/1
Uses, dosage, side effects and warnings for Oxycodone Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 10702-057-01 | 100 TABLET in 1 BOTTLE (10702-057-01) | Oct 18, 2013 |
| 10702-057-50 | 500 TABLET in 1 BOTTLE (10702-057-50) | Oct 18, 2013 |
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