NDC 0832-6084
Glatiramer Acetate 20 mg per 1 mL injection, solution
On the label: Upsher-Smith Laboratories, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| ScinoPharm Taiwan, Ltd. | Tainan, Taiwan | Makes it, makes the active ingredient, tests it and packages it | Serious problems, FDA actionJun 23, 2026 · 7 inspections, 1 with FDA action |
Product details
- Generic drug
- Glatiramer: every company that makes it
- Form
- injection, solution, subcutaneous
- Strength
- 20 mg per 1 mL
- Approval
- ANDA ANDA214741
- On the market since
- Jan 23, 2026
- Package NDCs
0832-6084-300832-6084-89- Official label
- DailyMed (National Library of Medicine), updated Jan 15, 2026
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