Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| USV Private Limited | Daman, India | Makes it, tests it, packages it, labels it and sterilizes it | Serious problems, FDA actionApr 17, 2026 · 8 inspections, 3 with FDA action |
Product details
- Generic drug
- Octreotide: every company that makes it
- Form
- injection
- Strength
- 1000 ug per 1 mL
- Approval
- ANDA ANDA203765
- On the market since
- Jan 1, 2019
- Package NDCs
76135-006-01- Official label
- DailyMed (National Library of Medicine), updated Sep 21, 2018
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