Home NDC 61504-080 ASPIRIN
Product NDC 61504-080
11-digit product format 615040080
Labeler code 61504
Product ID 61504-080_09086102-c886-f56b-e063-6294a90afe27
Type HUMAN OTC DRUG
Nonproprietary name ASPIRIN
Dosage form TABLET, DELAYED RELEASE
Route ORAL
Labeler AMERIFOODS TRADING COMPANY
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-10-30
Substance ASPIRIN
Active strength 81 mg/1
Pharmacologic classes Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Decreased Platelet Aggregation [PE], Decreased Prostaglandin Production [PE], Nonsteroidal Anti-inflammatory Drug [EPC], Platelet Aggregation Inhibitor [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base ASPIRIN
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ASPIRIN 81 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination R16CO5Y76E Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 308416 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 61504-080-01 ASPIRIN 120 in 1 BOTTLE, PLASTIC TABLET, DELAYED RELEASE 120 2 61504-080-01 ASPIRIN 1 in 1 CARTON TABLET, DELAYED RELEASE 1 2 61504-080-04 ASPIRIN 500 in 1 BOTTLE, PLASTIC TABLET, DELAYED RELEASE 500 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 61504-080 ASPIRIN TABLET, DELAYED RELEASE [AMERIFOODS TRADING COMPANY] 2 Current NDC, 3 package rows 20231101_f6cec280-17a5-5c5d-e053-6394a90a81aa.zip
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 83 · 1,657 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 61504-080-01 61504008001 1 BOTTLE, PLASTIC in 1 CARTON (61504-080-01) / 120 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC 2023-10-30 No No Current 61504-080-04 61504008004 500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (61504-080-04) 2023-10-30 No No Current