NDC11 63479030201

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
63479-0302-01	63479-0302
63479-0302-1	63479-0302
63479-302-01	63479-302

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 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
C02 FIBROZOLVE	APIS MELLIFICA, AURUM MURIATICUM NATRONATUM, BERBERIS VULGARIS, BOS TAURUS PITUITARUM POSTERIUM, CALCAREA FLUORICA, CALCAREA IODATA, CONIUM MACULATUM, FRAXINUS AMERICANA, HYDRASTIS CANADENSIS, HYDROFLUORICUM ACIDUM, LAPIS ALBUS, PANCREATINUM, SARCOLACTICUM ACIDUM, SEPIA, SULPHUR IODATUM, THIOSINAMINUM, THUJA OCCIDENTALIS, THYROIDINUM	Apex Energetics Inc.	b9e51df0-a9a3-30c1-e053-2a95a90a181c	2025-12-31	Warnings	Exact identifier ndc (package): 63479-0302-1 ndc (product): 63479-0302 ndc11 (package): 63479030201

Reported adverse events (FAERS/openFDA)#

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