FDA.reportPublic FDA data

NDC11 00173073900

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
00173-0739-000173-0739
00173-0739-0000173-0739
00173-739-0000173-739
0173-0739-000173-0739

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 LLCfee7d073-0b99-48f2-7985-0d8cf970894b2025-12-09Warnings, Adverse reactionsExact identifier
ndc (package): 0173-0739-00
ndc (product): 0173-0739
ndc11 (package): 00173073900

Reported adverse events (FAERS/openFDA)#

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