NDC 43386-433 – Oxycodone Hydrochloride
Oxycodone Hydrochloride 10 mg/1 · Tablet · Oral
Product NDC43386-433
Product details
- Brand name
- Oxycodone Hydrochloride
- Generic name
- Oxycodone Hydrochloride
- Labeler
- Lupin Pharmaceuticals,Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA204021
- Marketed since
- June 12, 2017
- Listing expires
- December 31, 2026
- Pharmacologic class
- Opioid Agonist
Active ingredients
- Oxycodone Hydrochloride 10 mg/1
Uses, dosage, side effects and warnings for Oxycodone Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 43386-433-01 | 100 TABLET in 1 BOTTLE (43386-433-01) | Jun 12, 2017 |
Recalls mentioning this NDC
- D-0358-2022 Jan 12, 2022 · Class III
Out-of-specification impurity test result observed at 18-month long term stability time point.
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