Home NDC 69618-015 ASPIRIN 325 MG EC
Product NDC 69618-015
11-digit product format 696180015
Labeler code 69618
Product ID 69618-015_2bc81112-204e-2514-e063-6394a90a80ed
Type HUMAN OTC DRUG
Nonproprietary name ASPIRIN
Dosage form TABLET
Route ORAL
Labeler Reliable 1 Laboratories LLC
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2015-11-01
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 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 325 MG EC
Listing expiration 2026-12-31 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 198467 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69618-015-01 ASPIRIN 325 MG EC 100 in 1 BOTTLE, PLASTIC TABLET 100 6 69618-015-10 ASPIRIN 325 MG EC 1000 in 1 BOTTLE, PLASTIC TABLET 1000 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69618-015 ASPIRIN 325 MG EC (ASPIRIN) TABLET [RELIABLE 1 LABORATORIES LLC] 6 Current NDC, Legacy NDC, 2 package rows 20250117_2ab8564f-f958-7512-e054-00144ff88e88.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 2 of 83 · 1,657 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 69618-015-01 69618001501 100 TABLET in 1 BOTTLE, PLASTIC (69618-015-01) 100 tablet 2015-11-01 0000-00-00 No No Current 69618-015-10 69618001510 1000 TABLET in 1 BOTTLE, PLASTIC (69618-015-10) 1000 tablet 2015-11-01 0000-00-00 No No Current