Home NDC 85237-1871-01 NDC 85237-1871-01 - Excedrin Migraine This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
Product NDC 85237-1871
Requested NDC 85237-1871-01
Package NDCs from labels 85237-1871-1, 85237-1871-2, 85237-1871-3, 85237-1871-4, 85237-1871-0, 85237-1871-7, 85237-1871-01
Manufacturer Select Consumer Group
Effective date 2026-07-03
Current FDA listing Not matched in FDA.report NDC product tables
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 85237-1871-1 ExcedrinMigraine 1 in 1 BLISTER PACK TABLET, FILM COATED 1 2 85237-1871-1 ExcedrinMigraine 2 in 1 POUCH TABLET, FILM COATED 2 2 85237-1871-2 ExcedrinMigraine 2 in 1 POUCH TABLET, FILM COATED 2 2 85237-1871-2 ExcedrinMigraine 2 in 1 BLISTER PACK TABLET, FILM COATED 2 2 85237-1871-3 ExcedrinMigraine 2 in 1 POUCH TABLET, FILM COATED 2 2 85237-1871-3 ExcedrinMigraine 25 in 1 BOX, UNIT-DOSE TABLET, FILM COATED 25 2 85237-1871-4 ExcedrinMigraine 50 in 1 BOX, UNIT-DOSE TABLET, FILM COATED 50 2 85237-1871-4 ExcedrinMigraine 2 in 1 POUCH TABLET, FILM COATED 2 2
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 76 of 327 · 6,538 matching rows.
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Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.