FDA NDC Directory · JSON-LD · Markdown
NDC 0054-0222 · HUMAN PRESCRIPTION DRUG · TABLET
| Labeler / Manufacturer | Hikma Pharmaceuticals USA Inc. |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA090749 |
| Dosage form / route | TABLET · ORAL |
| Active ingredients | QUETIAPINE FUMARATE (200 mg/1) |
| Marketing started | 20120327 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).