FDA NDC Directory · JSON-LD · Markdown
NDC 72189-673 · HUMAN PRESCRIPTION DRUG · TABLET
| Labeler / Manufacturer | Direct_Rx |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA211575 |
| Dosage form / route | TABLET · ORAL |
| Active ingredients | PREDNISONE (5 mg/1) |
| Marketing started | 20260409 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).