NDC 68462-772
Micafungin 20 mg per 1 mL injection, powder, lyophilized, for solution
On the label: Glenmark Pharmaceuticals Inc., USA.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Qilu Pharmaceutical (Hainan) Co., Ltd. | Haikou, China | Makes it and tests it | Problems found, fixed voluntarilyMay 19, 2023 · 5 inspections |
Product details
- Generic drug
- Micafungin: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intravenous
- Strength
- 20 mg per 1 mL
- Approval
- ANDA ANDA219273
- On the market since
- Jun 30, 2025
- Package NDCs
68462-772-0168462-772-10- Official label
- DailyMed (National Library of Medicine), updated Sep 9, 2025
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