NDC 76135-010
Octreotide Acetate 100 ug per 1 mL injection, solution
On the label: USV North America Inc..
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, solution
- Strength
- 100 ug per 1 mL
- Approval
- ANDA ANDA204669
- On the market since
- Feb 1, 2019
- Package NDCs
76135-010-01- Official label
- DailyMed (National Library of Medicine), updated Jan 7, 2019
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