NDC 76282-768
Paclitaxel 100mg per vial 100 mg per 20 mL injection, powder, lyophilized, for suspension
On the label: Exelan Pharmaceuticals, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Cipla Limited | Salcette, India | Makes it | Problems found, fixed voluntarilyJun 21, 2024 · 12 inspections, 2 with FDA action |
Product details
- Generic drug
- Paclitaxel: every company that makes it
- Form
- injection, powder, lyophilized, for suspension, intravenous
- Strength
- 100 mg per 20 mL
- Approval
- ANDA ANDA209657
- On the market since
- Aug 11, 2026
- Package NDCs
76282-768-09- Official label
- DailyMed (National Library of Medicine), updated Aug 10, 2026
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