Home NDC 68998-080 Aspirin
Product NDC 68998-080
11-digit product format 689980080
Labeler code 68998
Product ID 68998-080_27d8878f-b3ba-f99a-e063-6394a90a88ef
Type HUMAN OTC DRUG
Nonproprietary name ASPIRIN
Dosage form TABLET, DELAYED RELEASE
Route ORAL
Labeler Marc Glassman, Inc.
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2008-03-04
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 68998-080-01 Aspirin 120 in 1 BOTTLE, PLASTIC TABLET, DELAYED RELEASE 120 4 68998-080-01 Aspirin 1 in 1 CARTON TABLET, DELAYED RELEASE 1 4 68998-080-12 Aspirin 300 in 1 BOTTLE, PLASTIC TABLET, DELAYED RELEASE 300 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 68998-080 ASPIRIN TABLET, DELAYED RELEASE [MARC GLASSMAN, INC.] 4 Current NDC, Legacy NDC, 3 package rows 20241127_7990ca49-fb30-40fe-9ac4-48e89eac9bb2.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 Marketing end Sample Exclude flag Status 68998-080-01 68998008001 1 BOTTLE, PLASTIC in 1 CARTON (68998-080-01) / 120 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC 2008-03-04 0000-00-00 No No Current 68998-080-12 68998008012 300 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68998-080-12) 2013-06-18 0000-00-00 No No Current