NDC11 24208050402

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
24208-0504-02	24208-0504
24208-0504-2	24208-0504
24208-504-02	24208-504

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
Vyzulta	LATANOPROSTENE BUNOD	Bausch & Lomb Incorporated	60ce7900-a677-4fc2-88d0-1603baa9dbd4	2024-02-27	Warnings, Adverse reactions	Exact identifier ndc (package): 24208-504-02 ndc (product): 24208-504 ndc11 (package): 24208050402

Reported adverse events (FAERS/openFDA)#

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