NDC 76282-718
Lanreotide Acetate 60 mg per 0.2 mL injection
On the label: Exelan Pharmaceuticals, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Pharmathen International S.A. | Sapes, Greece | Makes it, tests it and packages it | Serious problems, FDA actionNov 21, 2025 · 2 inspections, 1 with FDA action |
Product details
- Generic drug
- Lanreotide: every company that makes it
- Form
- injection, subcutaneous
- Strength
- 60 mg per 0.2 mL
- Approval
- ANDA ANDA217193
- On the market since
- May 30, 2025
- Package NDCs
76282-718-67- Official label
- DailyMed (National Library of Medicine), updated Feb 1, 2025
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