FDA NDC Directory · JSON-LD · Markdown
NDC 0781-5560 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED
| Labeler / Manufacturer | Sandoz Inc |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA200889 |
| Dosage form / route | TABLET, FILM COATED · ORAL |
| Active ingredients | MONTELUKAST SODIUM (10 mg/1) |
| Marketing started | 20120803 |
| Package count | 3 |
Source: openFDA. Public-domain (CC0).