NDC 0944-0495
Flexbumin 0.05 g per 1 mL injection, solution
On the label: Takeda Pharmaceuticals America, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Baxalta Us Inc. | Los Angeles, CA, United States | Makes it | Not inspected on record |
| Baxalta Us Inc. | Round Lake, IL, United States | Makes it | Not inspected on record |
Product details
- Generic drug
- Albumin Human: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 0.05 g per 1 mL
- Approval
- BLA BLA101452
- On the market since
- Jul 31, 2014
- Package NDCs
0944-0495-050944-0495-06- Official label
- DailyMed (National Library of Medicine), updated Dec 18, 2024
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