FDA.reportPublic FDA data

NDC11 00220483741

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 NDCProduct root
00220-4837-4100220-4837
0220-4837-410220-4837

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 ยท 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Sulphur iodatumSULFUR IODIDEBoiron67261e30-7c2e-11e6-87ed-424c583030312023-02-20Exact identifier
ndc (package): 0220-4837-41
ndc (product): 0220-4837
ndc11 (package): 00220483741

Reported adverse events (FAERS/openFDA)#

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