NDC 70710-1725
Micafungin 20 mg per 1 mL injection, powder, lyophilized, for solution
On the label: Zydus Pharmaceuticals (USA) Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Zydus Lifesciences Limited | Vadodara, India | Makes it and tests it | Serious problems, FDA actionApr 23, 2024 · 2 inspections, 1 with FDA action |
Recalls
- Jul 2, 2024 · Class III · Zydus Pharmaceuticals (USA) Inc
Cross contamination with other products
Lots: Lot #: L300220, Exp. 05/31/2025.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
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 ANDA215241
- On the market since
- Apr 10, 2023
- Package NDCs
70710-1725-170710-1725-6- Official label
- DailyMed (National Library of Medicine), updated Jan 20, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?