NDC11 63323034101

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
63323-0341-01	63323-0341
63323-0341-1	63323-0341
63323-341-01	63323-341

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
Cefoxitin	CEFOXITIN SODIUM	Fresenius Kabi USA, LLC	2a9d1e7b-96ee-4e6c-a1e8-47b76b924422	2023-07-10	Warnings, Adverse reactions	Exact identifier ndc (product): 63323-341
Cefoxitin	CEFOXITIN SODIUM	Fresenius Kabi USA, LLC	d02170ff-65aa-48b8-a922-94271c46ffa7	2022-09-23	Warnings, Adverse reactions	Exact identifier ndc (package): 63323-341-01 ndc (product): 63323-341 ndc11 (package): 63323034101

Reported adverse events (FAERS/openFDA)#

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