Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Sanofi-Aventis Deutschland GmbH | Frankfurt am Main, Germany | Makes it, makes the active ingredient, tests it, packages it and labels it | Problems found, fixed voluntarilyMar 25, 2022 · 10 inspections, 1 with FDA action |
Product details
- Generic drug
- Insulin Glulisine: every company that makes it
- Form
- injection, solution, intravenous; subcutaneous
- Strength
- 100 [iU] per 1 mL
- Approval
- BLA BLA021629
- On the market since
- Feb 24, 2009
- Package NDCs
0088-2500-330088-2500-34- Official label
- DailyMed (National Library of Medicine), updated Nov 25, 2025
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