FDA NDC Directory · JSON-LD · Markdown
NDC 0480-2359 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE
| Labeler / Manufacturer | Teva Pharmaceuticals, Inc. |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA206210 |
| Dosage form / route | CAPSULE, EXTENDED RELEASE · ORAL |
| Active ingredients | TOPIRAMATE (200 mg/1) |
| Marketing started | 20230331 |
| Package count | 2 |
Source: openFDA. Public-domain (CC0).