NDC11 63323010802

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
63323-0108-02	63323-0108
63323-0108-2	63323-0108
63323-108-02	63323-108

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
Magnesium Sulfate in 5% Dextrose	MAGNESIUM SULFATE HEPTAHYDRATE	Fresenius Kabi USA, LLC	cea3f48b-375a-415a-a341-435c09719f7c	2024-04-24	Warnings, Adverse reactions	Exact identifier ndc (product): 63323-108
Magnesium Sulfate in 5% Dextrose	MAGNESIUM SULFATE HEPTAHYDRATE	Fresenius Kabi USA, LLC	fdffb339-89d1-4495-97b7-d9422d68b3d5	2024-04-24	Warnings, Adverse reactions	Exact identifier ndc (package): 63323-108-02 ndc (product): 63323-108 ndc11 (package): 63323010802

Reported adverse events (FAERS/openFDA)#

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