FDA.reportPublic FDA data

NDC11 00173071720

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
00173-0717-2000173-0717
00173-717-2000173-717
0173-0717-200173-0717

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
ADVAIR HFAFLUTICASONE PROPIONATE AND SALMETEROL XINAFOATEGlaxoSmithKline LLCdfaca6f9-3277-47b2-319d-1377917cb54c2024-05-23Warnings, Adverse reactionsExact identifier
ndc (package): 0173-0717-20
ndc (product): 0173-0717
ndc11 (package): 00173071720

Reported adverse events (FAERS/openFDA)#

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