FDA NDC Directory · JSON-LD · Markdown
NDC 68546-474 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE
| Generic name | deutetrabenazine |
|---|---|
| Labeler / Manufacturer | Teva Neuroscience, Inc. |
| Marketing category | New Drug Application (innovator) · App NDA216354 |
| Dosage form / route | TABLET, FILM COATED, EXTENDED RELEASE · ORAL |
| Active ingredients | DEUTETRABENAZINE (36 mg/1) |
| Marketing started | 20240529 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).