Home NDC 69790-616 ULINE Aspirin
Product NDC 69790-616
11-digit product format 697900616
Labeler code 69790
Product ID 69790-616_3e5d8d3a-9171-38b3-e063-6394a90aa024
Type HUMAN OTC DRUG
Nonproprietary name Aspirin
Dosage form TABLET, FILM COATED
Route ORAL
Labeler ULINE
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-07-20
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 ULINE Aspirin
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 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 69790-616-33 ULINE Aspirin 2 in 1 PACKET TABLET, FILM COATED 2 8 69790-616-33 ULINE Aspirin 50 in 1 BOX TABLET, FILM COATED 50 8
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69790-616 ULINE ASPIRIN (ASPIRIN) TABLET, COATED ULINE ASPIRIN (ASPIRIN) TABLET, FILM COATED [ULINE] 7 Current NDC, Legacy NDC, 2 package rows 20240829_9b2b053c-11e7-8169-e053-2995a90ae336.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 84 · 1,663 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 69790-616-33 69790061633 50 PACKET in 1 BOX (69790-616-33) / 2 TABLET, FILM COATED in 1 PACKET 50 packet 2020-07-20 0000-00-00 No No Current