NDC11 59883001604

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
59883-0016-04	59883-0016
59883-0016-4	59883-0016
59883-016-04	59883-016

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
FLUORIDEX	SODIUM FLUORIDE	DEN-MAT HOLDINGS, LLC.	5fd60635-4b66-15e3-e053-2991aa0ab23a	2019-02-28	Warnings, Adverse reactions	Exact identifier ndc (package): 59883-016-04 ndc (product): 59883-016 ndc11 (package): 59883001604

Reported adverse events (FAERS/openFDA)#

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