Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Jiangsu Hansoh Pharmaceutical Group Co., Ltd. FDF site | Lianyungang, China | Makes it, tests it, packages it and labels it | Serious problems, FDA actionApr 24, 2026 · 2 inspections, 1 with FDA action |
Product details
- Generic drug
- Fulvestrant: every company that makes it
- Form
- injection, intramuscular
- Strength
- 50 mg per 1 mL
- Approval
- ANDA ANDA214682
- On the market since
- Feb 10, 2022
- Package NDCs
0143-9022-010143-9022-02- Official label
- DailyMed (National Library of Medicine), updated Feb 10, 2025
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