NDC 23155-688
Octreotide Acetate 100 ug per 1 mL injection, solution
On the label: Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| USV Private Limited | Daman, India | Makes it and packages 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, intravenous; subcutaneous
- Strength
- 100 ug per 1 mL
- Approval
- ANDA ANDA204669
- On the market since
- May 25, 2022
- Package NDCs
23155-688-3123155-688-41- Official label
- DailyMed (National Library of Medicine), updated Dec 3, 2024
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