NDC 55150-308
Olanzapine 10 mg injection, powder, lyophilized, for solution
On the label: AuroMedics Pharma LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Eugia Pharma Specialities Limited | Sangareddy, India | Makes it, tests it and packages it | Serious problems, FDA actionFeb 6, 2026 · 7 inspections, 2 with FDA action |
Product details
- Generic drug
- Olanzapine: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intramuscular
- Strength
- 10 mg
- Approval
- ANDA ANDA210968
- On the market since
- Oct 22, 2020
- Package NDCs
55150-308-0155150-308-10- Official label
- DailyMed (National Library of Medicine), updated Feb 17, 2026
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