Oxycodone Hydrochloride
- Product NDC
- 71335-2126
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxycodone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA207418
- Marketing category
- ANDA
- Substance
- OXYCODONE HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 71335-2126-1 | 60 TABLET in 1 BOTTLE (71335-2126-1) | 20220718 | | No | Historical |
| 71335-2126-2 | 90 TABLET in 1 BOTTLE (71335-2126-2) | 20220718 | | No | Historical |
| 71335-2126-3 | 120 TABLET in 1 BOTTLE (71335-2126-3) | 20220718 | | No | Historical |
| 71335-2126-4 | 30 TABLET in 1 BOTTLE (71335-2126-4) | 20220718 | | No | Historical |
| 71335-2126-5 | 100 TABLET in 1 BOTTLE (71335-2126-5) | 20220718 | | No | Historical |
| 71335-2126-6 | 40 TABLET in 1 BOTTLE (71335-2126-6) | 20220718 | | No | Historical |
| 71335-2126-7 | 18 TABLET in 1 BOTTLE (71335-2126-7) | 20220718 | | No | Historical |
| 71335-2126-8 | 28 TABLET in 1 BOTTLE (71335-2126-8) | 20220718 | | No | Historical |
Related DailyMed Labels
| Set ID | Title | Manufacturer | Effective date | Type | Version |
|---|
| 27124cdf-a3e8-474c-9c1e-6fa48f6ddc05 | These highlights do not include all the information needed to use OXYCODONE HYDROCHLORIDE TABLETS safely and effectively. See full prescribing information for OXYCODONE HYDROCHLORIDE TABLETS. OXYCODONE HYDROCHLORIDE tablets, USP, for oral use, CII Initial U.S. Approval: 1950 | Bryant Ranch Prepack | 2023-11-14 | HUMAN PRESCRIPTION DRUG LABEL | 101 |