Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Sanofi-Aventis Deutschland GmbH | Frankfurt am Main, Germany | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyMar 25, 2022 · 10 inspections, 1 with FDA action |
| Sanofi-Aventis Singapore Pte. Ltd. | Singapore, Singapore | Makes the active ingredient and tests it | Problems found, fixed voluntarilyJun 13, 2025 · 6 inspections |
Product details
- Generic drug
- Enoxaparin: every company that makes it
- Form
- injection, intravenous; subcutaneous
- Strength
- 300 mg per 3 mL
- Approval
- NDA NDA020164
- On the market since
- Mar 29, 1993
- Package NDCs
0075-0626-03- Official label
- DailyMed (National Library of Medicine), updated May 28, 2026
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