Home NDC 72036-018 ASPIRIN
Product NDC 72036-018
11-digit product format 720360018
Labeler code 72036
Product ID 72036-018_58debdb5-fa55-ba6d-e063-6294a90a29f6
Type HUMAN OTC DRUG
Nonproprietary name ASPIRIN
Dosage form TABLET, COATED
Route ORAL
Labeler HARRIS TEETER
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2014-10-01
Substance ASPIRIN
Active strength 325 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
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ASPIRIN 325 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 212033 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 72036-018-11 ASPIRIN 100 in 1 BOTTLE, PLASTIC TABLET, COATED 100 5 72036-018-11 ASPIRIN 1 in 1 CARTON TABLET, COATED 1 5 72036-018-17 ASPIRIN 300 in 1 BOTTLE, PLASTIC TABLET, COATED 300 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72036-018 ASPIRIN TABLET, COATED [HARRIS TEETER] 5 Current NDC, Legacy NDC, 3 package rows 20241024_93cbd3cb-1072-89e6-e053-2995a90a2f15.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 13 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 Marketing end Sample Exclude flag Status 72036-018-11 72036001811 1 BOTTLE, PLASTIC in 1 CARTON (72036-018-11) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC 2014-11-01 0000-00-00 No No Current 72036-018-17 72036001817 300 TABLET, COATED in 1 BOTTLE, PLASTIC (72036-018-17) 2014-10-01 0000-00-00 No No Current