FDA NDC Directory · JSON-LD · Markdown
NDC 0115-1325 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE
| Generic name | FENOFIBRIC ACID |
|---|---|
| Labeler / Manufacturer | Amneal Pharmaceuticals of New York LLC |
| Marketing category | Abbreviated NDA (generic) · App ANDA200264 |
| Dosage form / route | CAPSULE, DELAYED RELEASE · ORAL |
| Active ingredients | FENOFIBRIC ACID (135 mg/1) |
| Marketing started | 20240601 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).