NDC 0517-0955
Olanzapine 10 mg per 2 mL injection, powder, lyophilized, for solution
On the label: American Regent, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| American Regent, Inc. | New Albany, OH, United States | Makes it | Problems found, fixed voluntarilyJan 29, 2026 · 5 inspections |
Product details
- Generic drug
- Olanzapine: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intramuscular
- Strength
- 10 mg per 2 mL
- Approval
- ANDA ANDA201741
- On the market since
- Jun 27, 2012
- Package NDCs
0517-0955-01- Official label
- DailyMed (National Library of Medicine), updated Mar 1, 2026
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