FDA NDC Directory · JSON-LD · Markdown
NDC 72189-519 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE
| Labeler / Manufacturer | Direct_Rx |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA209635 |
| Dosage form / route | TABLET, FILM COATED, EXTENDED RELEASE · ORAL |
| Active ingredients | QUETIAPINE FUMARATE (200 mg/1) |
| Marketing started | 20231101 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).