FDA NDC Directory · JSON-LD · Markdown
NDC 65862-875 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE
| Generic name | Quetiapine |
|---|---|
| Labeler / Manufacturer | Aurobindo Pharma Limited |
| Marketing category | Abbreviated NDA (generic) · App ANDA207655 |
| Dosage form / route | TABLET, FILM COATED, EXTENDED RELEASE · ORAL |
| Active ingredients | QUETIAPINE FUMARATE (200 mg/1) |
| Marketing started | 20171129 |
| Package count | 3 |
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