Home NDC 81533-600 NobleAid PAIN RELIEVER
Product NDC 81533-600
11-digit product format 815330600
Labeler code 81533
Product ID 81533-600_81abd590-b1d6-42fc-88f5-86fe0e50e781
Type HUMAN OTC DRUG
Nonproprietary name Aspirin
Dosage form TABLET, DELAYED RELEASE
Route ORAL
Labeler Noble Otc LLC
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-11-15
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 NobleAid PAIN RELIEVER
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 81533-600-10 NobleAid PAIN RELIEVER 100 in 1 BOTTLE TABLET, DELAYED RELEASE 100 4 81533-600-11 NobleAid PAIN RELIEVER 300 in 1 BOTTLE TABLET, DELAYED RELEASE 300 4 81533-600-30 NobleAid PAIN RELIEVER 1000 in 1 BOTTLE TABLET, DELAYED RELEASE 1000 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 81533-600 NOBLEAID PAIN RELIEVER (ASPIRIN) TABLET, DELAYED RELEASE [NOBLE OTC LLC] 4 Current NDC, Legacy NDC, 3 package rows 20241220_aa08e488-2f69-4d7e-86ba-ccfad563edcf.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 85 · 1,687 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 81533-600-10 81533060010 100 TABLET, DELAYED RELEASE in 1 BOTTLE (81533-600-10) 2021-11-15 2023-03-31 No No Current 81533-600-11 81533060011 300 TABLET, DELAYED RELEASE in 1 BOTTLE (81533-600-11) 2021-11-15 2023-03-31 No No Current 81533-600-30 81533060030 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (81533-600-30) 2021-11-15 2023-03-31 No No Current