Home NDC 50844-157 Aspirin
Product NDC 50844-157
11-digit product format 508440157
Labeler code 50844
Product ID 50844-157_fcddd023-fd54-4c26-ac79-8c8d6bfcb583
Type HUMAN OTC DRUG
Nonproprietary name Aspirin
Dosage form TABLET, FILM COATED
Route ORAL
Labeler L.N.K. International, Inc.
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 1996-02-10
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 Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 6 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2024-11-09 02:27 UTC · source 2024-11-08 excluded product product ad56d346431e…cc804d4bbf1e…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 50844-157-12 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded product product 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 50844-157-12 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 excluded product product 557ba5c1ecfa…9c80585c8c6e…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 50844-157-12 557ba5c1ecfa…9c80585c8c6e…
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
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 50844-157-11 Aspirin 60 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 60 18 50844-157-12 Aspirin 100 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 100 18 50844-157-97 Aspirin 300 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 300 18
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded ASPIRIN ACTIVE INGREDIENT R16CO5Y76E ASPIRIN TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.] 3 ASPIRIN ACTIVE MOIETY R16CO5Y76E ASPIRIN TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.] 3 HYPROMELLOSES INACTIVE INGREDIENT 3NXW29V3WO ASPIRIN TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.] 3 POLYETHYLENE GLYCOLS INACTIVE INGREDIENT 3WJQ0SDW1A ASPIRIN TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.] 3 PROPYLENE GLYCOL INACTIVE INGREDIENT 6DC9Q167V3 ASPIRIN TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.] 3 STARCH, CORN INACTIVE INGREDIENT O8232NY3SJ ASPIRIN TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.] 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 50844-157 ASPIRIN TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.] 14 Current NDC, Legacy NDC, 3 package rows 20250105_35005045-57b2-4ffe-ab70-22d570c1b161.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 31 of 79 · 1,579 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Pain Reliever PM Extra Strength ACETAMINOPHEN, DIPHENHYDRAMINE HCL Walgreen Company b4d8860b-d72f-4789-945e-1c6420a8efab 2025-12-02 Warnings Exact identifier application number: M013 Infants Pain and Fever ACETAMINOPHEN WALGREEN COMPANY f7b304d8-e37c-4ac6-b4a2-1797b92cb832 2025-12-01 Warnings Exact identifier application number: M013 Dye FreeInfants Pain and Fever ACETAMINOPHEN WALGREEN COMPANY 1a304570-88b6-4c16-a8b4-c064bfa5d95a 2025-12-01 Warnings Exact identifier application number: M013 Walgreen Severe Multi-Symptom Cough Cold Flu ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE WALGREENS b48d93fe-bb60-493f-8d1a-b2dc864203c4 2025-12-01 Warnings Exact identifier application number: M013 Multi Symptom Severe Cold and Nighttime Severe Cold and Cough ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DIPHENHYDRAMINE HCL, PHENYLEPHRINE HCL WALGREEN CO. 6c4ab613-a587-4ec4-9986-f1d000bc2d23 2025-12-01 Warnings Exact identifier application number: M013 WAG HBP Daytime and Nighttime Cold and Flu ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND DOXYLAMINE SUCCINATE WALGREENS CO. ac2f9ce8-e402-4451-a412-e99248a6ecbe 2025-12-01 Warnings Exact identifier application number: M013 Walgreen Day Time NightTime Cold and Flu Relief ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HYDROCHLORIDE,GUAIFENESIN WALGREENS CO. 5505217a-9679-4668-bdab-5d4553a47c56 2025-12-01 Warnings Exact identifier application number: M013 CAREALL Aspirin ASPIRIN New World Imports, Inc 58a371d4-1f00-4fda-8e08-80610c58505a 2025-12-01 Warnings Exact identifier application number: M013 CareALL Non Aspirin Extra Strength ACETAMINOPHEN New World Imports, Inc da05a1a1-35b4-4787-8c56-12e369f18ff0 2025-12-01 Warnings Exact identifier application number: M013 CareALL Acetaminophen Extra Strength ACETAMINOPHEN New World Imports, Inc 80a699b9-bf5c-4765-9e20-ccbc7e3ace7a 2025-12-01 Warnings Exact identifier application number: M013 CareALL Acetaminophen Extra Strength ACETAMINOPHEN New World Imports, Inc 66244cdb-2680-4fa8-890d-32aefd490038 2025-12-01 Warnings Exact identifier application number: M013 Family Wellness Childrens Pain Reliever 574 ACETAMINOPHEN Family Dollar Services, Inc. 902c1136-04d2-41f0-81c6-412663cdf378 2025-12-01 Warnings Exact identifier application number: M013 WalgreenChildrens Pain Fever ACETAMINOPHEN WALGREENS CO. 2f757cde-2604-4ca4-b54e-e444f3757cdd 2025-11-26 Warnings Exact identifier application number: M013 Walgreen Childrens Pain plus Fever ACETAMINOPHEN WALGREENS CO. 29ca2855-3c07-435d-a8e1-2997fcedd088 2025-11-26 Warnings Exact identifier application number: M013 Walgreens Childrens Cold plus Cough plus Runny Nose ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, AND DEXTROMETHORPHAN HYDROBROMIDE WALGREENS CO. 8714d4e6-3a3b-48c8-8ac1-51b933a2ceac 2025-11-26 Warnings Exact identifier application number: M013 Pain Reliever, 24/7 Life by 7-Eleven ACETAMINOPHEN TABLET, FILM COATED Lil' Drug Store Products, Inc. 44828b89-2563-b233-e063-6294a90ab124 2025-11-26 Warnings Exact identifier application number: M013 MEMBERS MARK ACETAMINOPHEN ACETAMINOPHEN Sam's West Inc 03e831d4-8060-4633-9d02-e77100063fb4 2025-11-26 Warnings Exact identifier application number: M013 Childrens Pain and Fever Dissolve Packs ACETAMINOPHEN WALGREENS CO. ea0f265f-7d64-4731-beda-0bb841dd1ad7 2025-11-25 Warnings Exact identifier application number: M013 Sore Throat Logenzes Sore Throat BENZOCAINE AND MENTHOL ATLANTIC BIOLOGICALS CORP. 71a80e13-bda3-40fb-b4e7-45e9985e707c 2025-11-24 Warnings Exact identifier application number: M013 better living brands childrens fever and pain reliver ACETAMINOPHEN BETTER LIVING BRANDS LLC c13ced61-c491-4fc2-b83f-78c6d9ad8546 2025-11-20 Warnings Exact identifier application number: M013
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 50844-157-11 50844015711 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-157-11) 1996-02-10 No No Current 50844-157-12 50844015712 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-157-12) 1996-02-10 0000-00-00 No No Current 50844-157-97 50844015797 300 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-157-97) 2025-11-24 No No Current