Home NDC 85237-1868 Excedrin
Product NDC 85237-1868
11-digit product format 852371868
Labeler code 85237
Product ID 85237-1868_46fa8b27-fe58-4382-e063-6394a90a8965
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen, Aspirin (NSAID), Caffeine
Dosage form TABLET, FILM COATED
Route ORAL
Labeler Select Consumer Group
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-01-01
Substance ACETAMINOPHEN; ASPIRIN; CAFFEINE
Active strength 250; 250; 65 mg/1; mg/1; mg/1
Pharmacologic classes Anti-Inflammatory Agents, Non-Steroidal [CS], Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Cyclooxygenase Inhibitors [MoA], Decreased Platelet Aggregation [PE], Decreased Prostaglandin Production [PE], Methylxanthine [EPC], Nonsteroidal Anti-inflammatory Drug [EPC], Platelet Aggregation Inhibitor [EPC], Xanthines [CS]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Excedrin
Brand name suffix Extra Strength Headache
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACETAMINOPHEN 250 mg/1 ASPIRIN 250 mg/1 CAFFEINE 65 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 362O9ITL9D Internal UNII lookup R16CO5Y76E Internal UNII lookup 3G6A5W338E Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 209468 Internal RxNorm lookup 308297 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 85237-1868-1 ExcedrinExtra Strength Headache 1 in 1 BLISTER PACK TABLET, FILM COATED 1 3 85237-1868-1 ExcedrinExtra Strength Headache 2 in 1 POUCH TABLET, FILM COATED 2 3 85237-1868-2 ExcedrinExtra Strength Headache 2 in 1 POUCH TABLET, FILM COATED 2 3 85237-1868-2 ExcedrinExtra Strength Headache 2 in 1 BLISTER PACK TABLET, FILM COATED 2 3 85237-1868-3 ExcedrinExtra Strength Headache 25 in 1 BOX, UNIT-DOSE TABLET, FILM COATED 25 3 85237-1868-3 ExcedrinExtra Strength Headache 2 in 1 POUCH TABLET, FILM COATED 2 3 85237-1868-6 ExcedrinExtra Strength Headache 2 in 1 POUCH TABLET, FILM COATED 2 3 85237-1868-6 ExcedrinExtra Strength Headache 50 in 1 BOX, UNIT-DOSE TABLET, FILM COATED 50 3
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 85 · 1,687 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 85237-1868-1 85237186801 1 POUCH in 1 BLISTER PACK (85237-1868-1) / 2 TABLET, FILM COATED in 1 POUCH 1 pouch 2024-01-01 No No Current 85237-1868-2 85237186802 2 POUCH in 1 BLISTER PACK (85237-1868-2) / 2 TABLET, FILM COATED in 1 POUCH 2 pouch 2024-01-01 No No Current 85237-1868-3 85237186803 25 POUCH in 1 BOX, UNIT-DOSE (85237-1868-3) / 2 TABLET, FILM COATED in 1 POUCH 25 pouch 2025-12-24 No No Current 85237-1868-6 85237186806 50 POUCH in 1 BOX, UNIT-DOSE (85237-1868-6) / 2 TABLET, FILM COATED in 1 POUCH 50 pouch 2025-12-24 No No Current