NDC 39822-1800
Olanzapine 10 mg per 2 mL injection, powder, for solution
On the label: XGen Pharmaceuticals DJB, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| UBI Pharma Inc. | Hukou, Taiwan | Makes it | Problems found, fixed voluntarilyJun 6, 2023 · 4 inspections |
Product details
- Generic drug
- Olanzapine: every company that makes it
- Form
- injection, powder, for solution, intramuscular
- Strength
- 10 mg per 2 mL
- Approval
- ANDA ANDA211072
- On the market since
- Aug 28, 2025
- Package NDCs
39822-1800-1- Official label
- DailyMed (National Library of Medicine), updated Mar 30, 2026
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