NDC 71288-567
Octreotide Acetate 100 ug per 1 mL injection, solution
On the label: Meitheal Pharmaceuticals Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Nanjing King-Friend Biochemical Pharmaceutical Co., Ltd (API and FDF Site) | Nanjing, China | Makes it | Problems found, fixed voluntarilyNov 10, 2023 · 3 inspections |
Product details
- Generic drug
- Octreotide: every company that makes it
- Form
- injection, solution, intravenous; subcutaneous
- Strength
- 100 ug per 1 mL
- Approval
- ANDA ANDA075957
- On the market since
- Feb 28, 2025
- Package NDCs
71288-567-0171288-567-02- Official label
- DailyMed (National Library of Medicine), updated Jan 16, 2025
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