NDC11 63323072902

This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.

Possible FDA NDC forms#

Package NDC, Product root table
Package NDC	Product root
63323-0729-02	63323-0729
63323-0729-2	63323-0729
63323-729-02	63323-729

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Micafungin	MICAFUNGIN SODIUM	Fresenius Kabi USA, LLC	dc5241be-4b85-4f04-8553-9819603373b8	2025-10-23	Warnings, Adverse reactions	Exact identifier ndc (product): 63323-729
Micafungin	MICAFUNGIN SODIUM	Fresenius Kabi USA, LLC	f8198836-4011-40b9-af25-466ae08727f8	2024-10-09	Warnings, Adverse reactions	Exact identifier ndc (package): 63323-729-02 ndc (product): 63323-729 ndc11 (package): 63323072902

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.