Home NDC 71679-104-10 PAIN RELIEVER
Product NDC 71679-104
Requested package NDC 71679-104-10
11-digit product format 716790104
Labeler code 71679
Product ID 71679-104_3770cc15-2376-9c49-e063-6394a90a5cf0
Type HUMAN OTC DRUG
Nonproprietary name aspirin 81 mg
Dosage form TABLET, DELAYED RELEASE
Route ORAL
Labeler Health Pharma USA, LLC
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-06-13
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 Additional Listing Data#
Finished product Yes
Brand name base PAIN RELIEVER
Listing expiration 2027-12-31 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 71679-104-05 PAIN RELIEVER 500 in 1 BOTTLE TABLET, DELAYED RELEASE 500 11 71679-104-10 PAIN RELIEVER 1000 in 1 BOTTLE TABLET, DELAYED RELEASE 1000 11
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71679-104 PAIN RELIEVER (ASPIRIN 81 MG) TABLET, DELAYED RELEASE [HEALTH PHARMA USA LLC] 3 Current NDC, Legacy NDC, 2 package rows 20231031_d60aed37-3a9e-46d1-e053-2995a90a1d1f.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 · 1,678 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 71679-104-10 71679010410 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (71679-104-10) 2022-01-21 0000-00-00 No No Current