NDC11 24208031710

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
24208-0317-10	24208-0317
24208-317-10	24208-317

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
Sulfacetamide Sodium and Prednisolone Sodium Phosphate	SULFACETAMIDE SODIUM AND PREDNISOLONE SODIUM PHOSPHATE	Bausch & Lomb Incoporated	9ec403eb-b5df-4e41-9e17-9d9d8ecac3f3	2023-08-01	Warnings, Adverse reactions	Exact identifier ndc (package): 24208-317-10 ndc (product): 24208-317 ndc11 (package): 24208031710

Reported adverse events (FAERS/openFDA)#

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