Oxycodone Hydrochloride
- Product NDC
- 76420-897
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxycodone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Asclemed USA, Inc.
- Application
- ANDA091490
- Marketing category
- ANDA
- Substance
- OXYCODONE HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 76420-897-01 | 100 TABLET in 1 BOTTLE, PLASTIC (76420-897-01) | 2025-01-08 | | No | Historical |
| 76420-897-10 | 10 TABLET in 1 BOTTLE, PLASTIC (76420-897-10) | 2025-01-08 | | No | Historical |
| 76420-897-20 | 20 TABLET in 1 BOTTLE, PLASTIC (76420-897-20) | 2025-01-08 | | No | Historical |
| 76420-897-30 | 30 TABLET in 1 BOTTLE, PLASTIC (76420-897-30) | 2025-01-08 | | No | Historical |
| 76420-897-60 | 60 TABLET in 1 BOTTLE, PLASTIC (76420-897-60) | 2025-01-08 | | No | Historical |
| 76420-897-90 | 90 TABLET in 1 BOTTLE, PLASTIC (76420-897-90) | 2025-01-08 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Oxycodone Hydrochloride | Asclemed USA, Inc. | ASCLEMED USA INC. DBA ENOVACHEM | 2025-01-08 | HUMAN PRESCRIPTION DRUG LABEL | 1 |