NDC 72162-1811 – Oxycodone Hydrochloride
Oxycodone Hydrochloride 5 mg/1 · Tablet · Oral
Product NDC72162-1811
Product details
- Brand name
- Oxycodone Hydrochloride
- Generic name
- Oxycodone
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA203638
- Marketed since
- October 30, 2012
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 72162-1811-0 | 30 TABLET in 1 BOTTLE (72162-1811-0) | May 30, 2024 |
| 72162-1811-1 | 60 TABLET in 1 BOTTLE (72162-1811-1) | May 30, 2024 |
| 72162-1811-2 | 90 TABLET in 1 BOTTLE (72162-1811-2) | May 30, 2024 |
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