FDA.reportPublic FDA data

NDC11 67877032001

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
67877-0320-0167877-0320
67877-0320-167877-0320
67877-320-0167877-320

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 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
IbuprofenIBUPROFENAscend Laboratories, LLC9ce036ef-a22d-4fca-9a62-1b10978f7b262026-06-05Boxed warning, Warnings, Adverse reactionsExact identifier
ndc (package): 67877-320-01
ndc (product): 67877-320
ndc11 (package): 67877032001
IBUPAKIBUPROFENPureTek Corporationa63f3857-92d1-0adf-e053-2995a90a3afa2023-01-11Boxed warning, Warnings, Adverse reactionsExact identifier
ndc (package): 67877-320-01
ndc11 (package): 67877032001

Reported adverse events (FAERS/openFDA)#

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