FDA NDC Directory · JSON-LD · Markdown
NDC 0480-3296 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE
| Labeler / Manufacturer | Teva Pharmaceuticals, Inc. |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA204982 |
| Dosage form / route | CAPSULE, EXTENDED RELEASE · ORAL |
| Active ingredients | PHENTERMINE HYDROCHLORIDE (7.5 mg/1) TOPIRAMATE (46 mg/1) |
| Marketing started | 20250507 |
| Package count | 1 |
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