NDC 31722-917 – Oxycodone Hydrochloride
Oxycodone Hydrochloride 15 mg/1 · Tablet · Oral
Product NDC31722-917
Product details
- Brand name
- Oxycodone Hydrochloride
- Generic name
- Oxycodone Hydrochloride
- Labeler
- Camber Pharmaceuticals Inc
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA207418
- Marketed since
- August 8, 2017
- Listing expires
- December 31, 2027
- Pharmacologic class
- Opioid Agonist
Active ingredients
- Oxycodone Hydrochloride 15 mg/1
Uses, dosage, side effects and warnings for Oxycodone Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 31722-917-01 | 100 TABLET in 1 BOTTLE (31722-917-01) | Aug 8, 2017 |
| 31722-917-05 | 500 TABLET in 1 BOTTLE (31722-917-05) | Aug 8, 2017 |
Recalls mentioning this NDC
- D-0248-2018 Feb 7, 2018 · Class III
Labeling; Label Error Not Elsewhere Classified; label missing controlled substance CII symbol
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