FDA NDC Directory · JSON-LD · Markdown
NDC 0406-8520 · HUMAN PRESCRIPTION DRUG · TABLET
| Generic name | oxycodone hydrochloride |
|---|---|
| Labeler / Manufacturer | SpecGx LLC |
| Marketing category | Abbreviated NDA (generic) · App ANDA076758 |
| Dosage form / route | TABLET · ORAL |
| Active ingredients | OXYCODONE HYDROCHLORIDE (20 mg/1) |
| Marketing started | 20211012 |
| Package count | 3 |
Source: openFDA. Public-domain (CC0).