NDC11 73352010101

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
73352-0101-01	73352-0101
73352-0101-1	73352-0101
73352-101-01	73352-101

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
FENOFIBRATE	FENOFIBRATE	Trifluent Pharma LLC	3c3539e4-bc4a-8152-e063-6294a90ab55c	2025-08-12	Warnings, Adverse reactions	Exact identifier ndc (package): 73352-101-01 ndc (product): 73352-101 ndc11 (package): 73352010101

Reported adverse events (FAERS/openFDA)#

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