NDC 70095-080
Eribulin Mesylate 0.5 mg per 1 mL injection
On the label: Sun Pharmaceutical Industries Limited.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Lianyungang, China | Makes it, tests it and packages it | Problems found, fixed voluntarilyJan 30, 2026 · 2 inspections |
Product details
- Generic drug
- Eribulin: every company that makes it
- Form
- injection, intravenous
- Strength
- 0.5 mg per 1 mL
- Approval
- ANDA ANDA218743
- On the market since
- May 15, 2025
- Package NDCs
70095-080-01- Official label
- DailyMed (National Library of Medicine), updated May 6, 2025
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