Home NDC 42507-080 Aspirin 81 mg
Product NDC 42507-080
11-digit product format 425070080
Labeler code 42507
Product ID 42507-080_48494033-500a-1348-e063-6394a90a8cb2
Type HUMAN OTC DRUG
Nonproprietary name ASPIRIN
Dosage form TABLET, DELAYED RELEASE
Route ORAL
Labeler HYVEE INC
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-10-22
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 2027-12-31
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 81 mg
Listing expiration 2027-12-31 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 42507-080-01 Aspirin 81 mg 120 in 1 BOTTLE, PLASTIC TABLET, DELAYED RELEASE 120 3 42507-080-01 Aspirin 81 mg 120 in 1 CARTON TABLET, DELAYED RELEASE 120 3 42507-080-04 Aspirin 81 mg 500 in 1 BOTTLE, PLASTIC TABLET, DELAYED RELEASE 500 3 42507-080-08 Aspirin 81 mg 2 in 1 CARTON TABLET, DELAYED RELEASE 2 3 42507-080-08 Aspirin 81 mg 120 in 1 BOTTLE, PLASTIC TABLET, DELAYED RELEASE 120 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 78 of 79 · 1,579 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 42507-080-01 42507008001 120 BOTTLE, PLASTIC in 1 CARTON (42507-080-01) / 120 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC 2026-10-13 No No Current 42507-080-04 42507008004 500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (42507-080-04) 2026-01-13 No No Current 42507-080-08 42507008008 2 BOTTLE, PLASTIC in 1 CARTON (42507-080-08) / 120 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC 2025-10-22 No No Current