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
- 72303-0838_4d2e9776-65f4-cb00-e063-6394a90a1bf7
- Product NDC
- 72303-0838
- Form
- TABLET
- Composition / generic term
- Olanzapine
- Labeler
- HEC Pharm USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20181130
- Source listing expiry
- 20271231
Source-listed ingredients
- OLANZAPINE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE, PLASTIC (72303-0838-1) · 72303-0838-1
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →