FDA NDC Directory · JSON-LD · Markdown
NDC 71288-558 · HUMAN PRESCRIPTION DRUG · KIT
| Labeler / Manufacturer | Meitheal Pharmaceuticals Inc. |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA214540 |
| Dosage form / route | KIT · SUBCUTANEOUS |
| Active ingredients | — |
| Marketing started | 20240424 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).