FDA NDC Directory · JSON-LD · Markdown
NDC 0002-4453 · HUMAN PRESCRIPTION DRUG · TABLET, ORALLY DISINTEGRATING
| Generic name | Olanzapine |
|---|---|
| Labeler / Manufacturer | Eli Lilly and Company |
| Marketing category | New Drug Application (innovator) · App NDA021086 |
| Dosage form / route | TABLET, ORALLY DISINTEGRATING · ORAL |
| Active ingredients | OLANZAPINE (5 mg/1) |
| Marketing started | 20000601 |
| Marketing ended | 20260630 |
| Package count | 1 |
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