NDC 0088-2219
Lantus Solostar 100 [iU] per 1 mL injection, solution
On the label: sanofi-aventis U.S. LLC.
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 Glargine: every company that makes it
- Form
- injection, solution, subcutaneous
- Strength
- 100 [iU] per 1 mL
- Approval
- BLA BLA021081
- On the market since
- Sep 23, 2009
- Package NDCs
0088-2219-000088-2219-010088-2219-05- Official label
- DailyMed (National Library of Medicine), updated Jun 2, 2025
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