FDA NDC Directory · JSON-LD · Markdown
NDC 59676-702 · HUMAN PRESCRIPTION DRUG · TABLET
| Generic name | Bedaquiline Fumarate |
|---|---|
| Labeler / Manufacturer | Janssen Products, LP |
| Marketing category | New Drug Application (innovator) · App NDA204384 |
| Dosage form / route | TABLET · ORAL |
| Active ingredients | BEDAQUILINE FUMARATE (20 mg/1) |
| Marketing started | 20200527 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).