Oxycodone Hydrochloride
- Product NDC
- 72162-1812
- 11-digit product format
- 721621812
- Labeler code
- 72162
- Product ID
- 72162-1812_76f5ec67-3129-4514-b9fa-fd389c57a216
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxycodone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA203638
- Marketing category
- ANDA
- Marketing start
- 2012-10-30
- Substance
- OXYCODONE HYDROCHLORIDE
- Active strength
- 30 mg/1
- Pharmacologic classes
- Full Opioid Agonists [MoA], Opioid Agonist [EPC]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| C1ENJ2TE6C | OXYCODONE HYDROCHLORIDE | 124-90-3 | OXYCODONE HYDROCHLORIDE |
| CD35PMG570 | OXYCODONE | 76-42-6 | Oxycodone |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1812-0 | 72162181200 | 60 TABLET in 1 BOTTLE (72162-1812-0) | 60 tablet | 2024-05-30 | No | No | Historical |
| 72162-1812-1 | 72162181201 | 90 TABLET in 1 BOTTLE (72162-1812-1) | 90 tablet | 2024-05-30 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Oxycodone Hydrochloride | Bryant Ranch Prepack | 2024-05-30 | HUMAN PRESCRIPTION DRUG LABEL | 101 |