NDC 68180-738
decitabine 50 mg per 20 mL injection, powder, lyophilized, for solution
On the label: Lupin Pharmaceuticals, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Shilpa Medicare Limited | Mahabubnagar, India | Makes it | Serious problems, FDA actionFeb 25, 2020 · 6 inspections, 1 with FDA action |
Product details
- Generic drug
- Decitabine: every company that makes it
- Form
- injection, powder, lyophilized, for solution
- Strength
- 50 mg per 20 mL
- Approval
- ANDA ANDA210756
- On the market since
- Dec 6, 2019
- Package NDCs
68180-738-01- Official label
- DailyMed (National Library of Medicine), updated Dec 14, 2023
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