Home NDC 72090-034 Aspirin Pain reliver
Product NDC 72090-034
11-digit product format 720900034
Labeler code 72090
Product ID 72090-034_ee1c0ed7-e39d-4d8b-b7b8-fb10ce496321
Type HUMAN OTC DRUG
Nonproprietary name Aspirin
Dosage form TABLET
Route ORAL
Labeler Pioneer Life Sciences, LLC
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-09-12
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 Pain reliver
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 72090-034-01 Aspirin Pain reliver 500 in 1 BOTTLE TABLET 500 2 72090-034-02 Aspirin Pain reliver 1000 in 1 BOTTLE TABLET 1000 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72090-034 ASPIRIN PAIN RELIVER (ASPIRIN) TABLET [PIONEER LIFE SCIENCES, LLC] 1 Current NDC, 2 package rows 20240913_8dc29957-2ac1-47f8-89fd-a6bcf97ee3d3.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 59 of 79 · 1,579 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 72090-034-01 72090003401 500 TABLET in 1 BOTTLE (72090-034-01) 500 tablet 2024-09-12 No No Current 72090-034-02 72090003402 1000 TABLET in 1 BOTTLE (72090-034-02) 1000 tablet 2024-09-12 No No Current