← FDA Drug Approvals (Drugs@FDA)
MICAFUNGIN IN SODIUM CHLORIDE 0.9%
NDA · New Drug Application · Sponsor: BAXTER HLTHCARE CORP · Approved 2023-09-29
Drug application
- FDA Application #
NDA216142
- Application type
- New Drug Application
- Brand name
- MICAFUNGIN IN SODIUM CHLORIDE 0.9%
- Generic name
- MICAFUNGIN IN SODIUM CHLORIDE
- Active ingredients
- MICAFUNGIN SODIUM
- Dosage form
- SOLUTION
- Route
- INTRAVENOUS
- Marketing status
- Prescription
- Sponsor
- BAXTER HLTHCARE CORP
- Manufacturer
- Baxter Healthcare Corporation
- First approval
- 2023-09-29
Source
- Authoritative
- Drugs@FDA application overview
- Machine
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