United States · FDA National Drug Code directory
Olanzapine
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 0143-9199_c6ff3b59-0671-447c-b602-3c97e844d6e8
- Product NDC
- 0143-9199
- Form
- INJECTION, POWDER, FOR SOLUTION
- Composition / generic term
- Olanzapine
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250918
- Source listing expiry
- 20271231
Source-listed ingredients
- OLANZAPINE — 10 mg/2mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL in 1 CARTON (0143-9199-01) / 2 mL in 1 VIAL · 0143-9199-01
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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