NDC 68001-629
Doxorubicin Hydrochloride 2 mg per 1 mL injection, suspension, liposomal
On the label: BluePoint Laboratories..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Fordoz Pharma Corporation | East Windsor, NJ, United States | Makes it, tests it and packages it | Serious problems, FDA actionNov 12, 2025 · 1 inspection, 1 with FDA action |
Product details
- Generic drug
- Doxorubicin: every company that makes it
- Form
- injection, suspension, liposomal, intravenous
- Strength
- 2 mg per 1 mL
- Approval
- ANDA ANDA215178
- On the market since
- Jan 7, 2025
- Package NDCs
68001-629-2668001-629-36- Official label
- DailyMed (National Library of Medicine), updated Dec 11, 2024
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