NDC 72162-1334 – Oxycodone Hydrochloride
Oxycodone Hydrochloride 5 mg/1 · Tablet · Oral
Product NDC72162-1334
Product details
- Brand name
- Oxycodone Hydrochloride
- Generic name
- Oxycodone Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA091490
- Marketed since
- September 8, 2014
- Listing expires
- December 31, 2027
- Pharmacologic class
- Opioid Agonist
Active ingredients
- Oxycodone Hydrochloride 5 mg/1
Uses, dosage, side effects and warnings for Oxycodone Hydrochloride →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 72162-1334-2 | 20 TABLET in 1 BOTTLE (72162-1334-2) | Apr 7, 2026 |
| 72162-1334-3 | 30 TABLET in 1 BOTTLE (72162-1334-3) | Apr 7, 2026 |
| 72162-1334-6 | 60 TABLET in 1 BOTTLE (72162-1334-6) | Apr 7, 2026 |
| 72162-1334-9 | 90 TABLET in 1 BOTTLE (72162-1334-9) | Apr 7, 2026 |
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