FDA NDC Directory · JSON-LD · Markdown
NDC 0173-0736 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED
| Generic name | sumatriptan |
|---|---|
| Labeler / Manufacturer | GlaxoSmithKline LLC |
| Marketing category | New Drug Application (innovator) · App NDA020132 |
| Dosage form / route | TABLET, FILM COATED · ORAL |
| Active ingredients | SUMATRIPTAN SUCCINATE (50 mg/1) |
| Marketing started | 20031217 |
| Package count | 1 |
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