FDA.reportPublic FDA data

NDC11 00173073601

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
00173-0736-0100173-0736
00173-0736-100173-0736
00173-736-0100173-736
0173-0736-010173-0736

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
IMITREXSUMATRIPTANGlaxoSmithKline LLC584abe73-8290-4484-ff8e-5890831c095e2025-12-09Warnings, Adverse reactionsExact identifier
ndc (package): 0173-0736-01
ndc (product): 0173-0736
ndc11 (package): 00173073601

Reported adverse events (FAERS/openFDA)#

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