NDC 0143-9199
Olanzapine 10 mg per 2 mL injection, powder, for solution
On the label: Hikma Pharmaceuticals USA Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Qilu Pharmaceutical Co., Ltd. (Biological Industrial Park) | Jinan, China | Makes it and tests it | Problems found, fixed voluntarilyMay 8, 2026 · 1 inspection |
Product details
- Generic drug
- Olanzapine: every company that makes it
- Form
- injection, powder, for solution, intramuscular
- Strength
- 10 mg per 2 mL
- Approval
- ANDA ANDA218116
- On the market since
- Sep 18, 2025
- Package NDCs
0143-9199-01- Official label
- DailyMed (National Library of Medicine), updated Aug 25, 2026
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