OXYCODONE HYDROCHLORIDE
- Product NDC
- 60760-955
- 11-digit product format
- 607600955
- Labeler code
- 60760
- Product ID
- 60760-955_3cd0143b-2802-e698-e063-6294a90aa581
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- OXYCODONE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- ST. MARY'S MEDICAL PARK PHARMACY
- Application
- ANDA091393
- Marketing category
- ANDA
- Marketing start
- 2013-10-18
- Substance
- OXYCODONE HYDROCHLORIDE
- Active strength
- 10 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 |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 60760-955-30 | 60760095530 | 30 TABLET in 1 BOTTLE, PLASTIC (60760-955-30) | 30 tablet | 2025-08-20 | No | No | Historical |
| 60760-955-60 | 60760095560 | 60 TABLET in 1 BOTTLE, PLASTIC (60760-955-60) | 60 tablet | 2025-08-20 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| OXYCODONE HYDROCHLORIDE | ST. MARY'S MEDICAL PARK PHARMACY | 2025-08-20 | HUMAN PRESCRIPTION DRUG LABEL | 1 |