FDA NDC Directory · JSON-LD · Markdown
NDC 0002-4117 · HUMAN PRESCRIPTION DRUG · TABLET
| Generic name | Olanzapine |
|---|---|
| Labeler / Manufacturer | Eli Lilly and Company |
| Marketing category | New Drug Application (innovator) · App NDA020592 |
| Dosage form / route | TABLET · ORAL |
| Active ingredients | OLANZAPINE (10 mg/1) |
| Marketing started | 19961001 |
| Marketing ended | 20260524 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).