NDC 68084-354 – Oxycodone Hydrochloride
Oxycodone Hydrochloride 5 mg/1 · Tablet · Oral
Product NDC68084-354
Product details
- Brand name
- Oxycodone Hydrochloride
- Generic name
- Oxycodone Hydrochloride
- Labeler
- American Health Packaging
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA091393
- Marketed since
- December 4, 2009
- Listing expires
- December 31, 2026
- Pharmacologic class
- Opioid Agonist
Active ingredients
- Oxycodone Hydrochloride 5 mg/1
Uses, dosage, side effects and warnings for Oxycodone Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 68084-354-01 | 100 BLISTER PACK in 1 CARTON (68084-354-01) / 1 TABLET in 1 BLISTER PACK (68084-354-11) | Dec 4, 2009 |
Recalls mentioning this NDC
- D-0338-2026 Feb 18, 2026 · Class II
Defective container: card seal defects (weak/non-existent seals), leading to the tablets falling out of their cavities.
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- 65162-048 Oxycodone Hydrochloride 10 mg/1 · Tablet · Amneal Pharmaceuticals LLC
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