Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Fresenius Kabi USA, LLC | Melrose Park, IL, United States | Makes it and tests it | Problems found, fixed voluntarilyAug 24, 2023 · 13 inspections, 2 with FDA action |
Product details
- Generic drug
- Octreotide: every company that makes it
- Form
- injection, solution, intravenous; subcutaneous
- Strength
- 1000 ug per 1 mL
- Approval
- ANDA ANDA077450
- On the market since
- Mar 14, 2006
- Package NDCs
63323-379-05- Official label
- DailyMed (National Library of Medicine), updated May 7, 2024
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?