Oxycodone Hydrochloride
- Product NDC
- 72162-1749
- 11-digit product format
- 721621749
- Labeler code
- 72162
- Product ID
- 72162-1749_acd2a06e-f3f7-4aef-85b3-e17d651eac28
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxycodone Hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA204979
- Marketing category
- ANDA
- Marketing start
- 2015-10-13
- Substance
- OXYCODONE HYDROCHLORIDE
- Active strength
- 5 mg/5mL
- 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 |
|---|
| 72162-1749-2 | 72162174902 | 1 BOTTLE in 1 CARTON (72162-1749-2) / 473 mL in 1 BOTTLE | 1 bottle | 2015-10-13 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Oxycodone Hydrochloride | Bryant Ranch Prepack | 2024-07-17 | HUMAN PRESCRIPTION DRUG LABEL | 104 |