NDC11 59651020101

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
59651-0201-01	59651-0201
59651-0201-1	59651-0201
59651-201-01	59651-201

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	Aurobindo Pharma Limited	05957860-eab3-4172-9877-455540d0c922	2021-09-08	Warnings, Adverse reactions	Exact identifier ndc (package): 59651-201-01 ndc (product): 59651-201 ndc11 (package): 59651020101

Reported adverse events (FAERS/openFDA)#

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