NDC11 80353090001

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
80353-0900-01	80353-0900
80353-0900-1	80353-0900
80353-900-01	80353-900

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
URICOZEN	GOUT RECOVERY, JOINT PAIN AND INFLAMMATION RELIEF, AND GOUT CRYSTAL DISSOLUTION	HCBIOPHARM	0bfb4b71-8392-15fa-e063-6394a90a771b	2026-03-30	Warnings	Exact identifier ndc (package): 80353-900-01 ndc (product): 80353-900 ndc11 (package): 80353090001

Reported adverse events (FAERS/openFDA)#

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