Oxycodone Hydrochloride
- Product NDC
- 72162-1811
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxycodone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA203638
- Marketing category
- ANDA
- Substance
- OXYCODONE HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 72162-1811-0 | 30 TABLET in 1 BOTTLE (72162-1811-0) | 2024-05-30 | | No | Historical |
| 72162-1811-1 | 60 TABLET in 1 BOTTLE (72162-1811-1) | 2024-05-30 | | No | Historical |
| 72162-1811-2 | 90 TABLET in 1 BOTTLE (72162-1811-2) | 2024-05-30 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Oxycodone Hydrochloride | Bryant Ranch Prepack | 2024-05-30 | HUMAN PRESCRIPTION DRUG LABEL | 101 |