Home NDC 50844-675 Aspi-Cor
Product NDC 50844-675
11-digit product format 508440675
Labeler code 50844
Product ID 50844-675_5a3de209-0779-4fa6-9bbb-dfea9c0abb45
Type HUMAN OTC DRUG
Nonproprietary name Aspirin
Dosage form TABLET, DELAYED RELEASE
Route ORAL
Labeler L.N.K. International, Inc.
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2015-02-03
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 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 Aspi-Cor
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 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 308416 Internal RxNorm lookup 1600991 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 50844-675-03 Aspi-Cor 10 in 1 BOTTLE, PLASTIC TABLET, DELAYED RELEASE 10 16 50844-675-26 Aspi-Cor 85000 in 1 BAG TABLET, DELAYED RELEASE 85000 16 50844-675-26 Aspi-Cor 1 in 1 BOX TABLET, DELAYED RELEASE 1 16 50844-675-32 Aspi-Cor 120 in 1 BOTTLE, PLASTIC TABLET, DELAYED RELEASE 120 16
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded ASPIRIN ACTIVE INGREDIENT R16CO5Y76E ASPI-COR (ASPIRIN) TABLET, COATED [L.N.K. INTERNATIONAL, INC.] 3 ASPIRIN ACTIVE MOIETY R16CO5Y76E ASPI-COR (ASPIRIN) TABLET, COATED [L.N.K. INTERNATIONAL, INC.] 3 CELLULOSE, MICROCRYSTALLINE INACTIVE INGREDIENT OP1R32D61U ASPI-COR (ASPIRIN) TABLET, COATED [L.N.K. INTERNATIONAL, INC.] 3 CROSCARMELLOSE SODIUM INACTIVE INGREDIENT M28OL1HH48 ASPI-COR (ASPIRIN) TABLET, COATED [L.N.K. INTERNATIONAL, INC.] 3 D&C YELLOW NO. 10 INACTIVE INGREDIENT 35SW5USQ3G ASPI-COR (ASPIRIN) TABLET, COATED [L.N.K. INTERNATIONAL, INC.] 3 FD&C YELLOW NO. 6 INACTIVE INGREDIENT H77VEI93A8 ASPI-COR (ASPIRIN) TABLET, COATED [L.N.K. INTERNATIONAL, INC.] 3 FERROSOFERRIC OXIDE INACTIVE INGREDIENT XM0M87F357 ASPI-COR (ASPIRIN) TABLET, COATED [L.N.K. INTERNATIONAL, INC.] 3 HYPROMELLOSES INACTIVE INGREDIENT 3NXW29V3WO ASPI-COR (ASPIRIN) TABLET, COATED [L.N.K. INTERNATIONAL, INC.] 3 POLYDEXTROSE INACTIVE INGREDIENT VH2XOU12IE ASPI-COR (ASPIRIN) TABLET, COATED [L.N.K. INTERNATIONAL, INC.] 3 POLYETHYLENE GLYCOLS INACTIVE INGREDIENT 3WJQ0SDW1A ASPI-COR (ASPIRIN) TABLET, COATED [L.N.K. INTERNATIONAL, INC.] 3 PROPYLENE GLYCOL INACTIVE INGREDIENT 6DC9Q167V3 ASPI-COR (ASPIRIN) TABLET, COATED [L.N.K. INTERNATIONAL, INC.] 3 SHELLAC INACTIVE INGREDIENT 46N107B71O ASPI-COR (ASPIRIN) TABLET, COATED [L.N.K. INTERNATIONAL, INC.] 3 SODIUM BICARBONATE INACTIVE INGREDIENT 8MDF5V39QO ASPI-COR (ASPIRIN) TABLET, COATED [L.N.K. INTERNATIONAL, INC.] 3 SODIUM LAURYL SULFATE INACTIVE INGREDIENT 368GB5141J ASPI-COR (ASPIRIN) TABLET, COATED [L.N.K. INTERNATIONAL, INC.] 3 STARCH, CORN INACTIVE INGREDIENT O8232NY3SJ ASPI-COR (ASPIRIN) TABLET, COATED [L.N.K. INTERNATIONAL, INC.] 3 TALC INACTIVE INGREDIENT 7SEV7J4R1U ASPI-COR (ASPIRIN) TABLET, COATED [L.N.K. INTERNATIONAL, INC.] 3 TITANIUM DIOXIDE INACTIVE INGREDIENT 15FIX9V2JP ASPI-COR (ASPIRIN) TABLET, COATED [L.N.K. INTERNATIONAL, INC.] 3 TRIACETIN INACTIVE INGREDIENT XHX3C3X673 ASPI-COR (ASPIRIN) TABLET, COATED [L.N.K. INTERNATIONAL, INC.] 3 TRIETHYL CITRATE INACTIVE INGREDIENT 8Z96QXD6UM ASPI-COR (ASPIRIN) TABLET, 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 50844-675 ASPI-COR (ASPIRIN) TABLET, DELAYED RELEASE [L.N.K. INTERNATIONAL, INC.] 15 Current NDC, Legacy NDC, 4 package rows 20240829_9f919a48-ffd8-49fa-b6fd-ec71cc12e64b.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 54 of 79 · 1,579 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join NOTTS - Pain Relief PM ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE VIVUNT PHARMA LLC e6754f62-e3b2-773f-e053-2a95a90ad36a 2024-12-02 Warnings Exact identifier application number: M013 Pain Relief ACETAMINOPHEN AAA Pharmaceutical, Inc. a891896d-c9fa-4448-915a-e6b531157d22 2024-12-02 Warnings Exact identifier application number: M013 Pain Relief Extra Strength ACETAMINOPHEN SAFEWAY d2d15e06-e9eb-3d2b-e053-2995a90a1cec 2024-12-02 Warnings Exact identifier application number: M013 Pain Relief Regular Strength ACETAMINOPHEN TopCo Associates LLC c2d33352-431c-4683-a4fa-a54437e7b8d2 2024-12-02 Warnings Exact identifier application number: M013 Pain Relief Extra Strength ACETAMINOPHEN TopCo Associates LLC bdb01b3e-ad34-4003-9b9a-e83a2c0e90bb 2024-12-02 Warnings Exact identifier application number: M013 Aspirin 81mg Adult Low Dose ASPIRIN TopCare 14d010fb-c4a1-4c3d-942f-58719727bfc0 2024-12-02 Warnings Exact identifier application number: M013 Acetaminophen ACETAMINOPHEN CVS Pharmacy, Inc c4473ee6-4e01-1ec2-e053-2995a90ac513 2024-12-02 Warnings Exact identifier application number: M013 Aspirin ASPIRIN Proficient Rx LP 9c186289-e309-45e8-8934-1d0eae0375c2 2024-12-01 Warnings Exact identifier application number: M013 Childrens Chewable Acetaminophen ACETAMINOPHEN GERI-CARE PHARMACEUTICAL CORP 22f63d62-c941-5b8f-e063-6394a90aeecd 2024-11-28 Warnings Exact identifier application number: M013 Extra Strength Acetaminophen ACETAMINOPHEN Geri-Care Pharmaceutical Corp 7a7b6318-b7d6-31b1-e053-2991aa0abf25 2024-11-28 Warnings Exact identifier application number: M013 Extra Strength Pain Reliever PM ACETAMINOPHEN, DIPHENHYDRAMINE HCL INGLES MARKETS, INC. 27fd288e-c07a-617f-e063-6394a90a17a4 2024-11-28 Warnings Exact identifier application number: M013 BAYER Aspirin Original, TRAVEL BASIX ASPIRIN Lil' Drug Store Products, Inc. 7f5d9ebe-8119-49a2-9380-eca18a5e5e85 2024-11-27 Warnings Exact identifier application number: M013 EXCEDRIN MIGRAINE ACETAMINOPHEN, ASPIRIN (NSAID) AND CAFFEINE Jones Healthcare Group - Packaging Services, Inc c4168e4d-3dfc-4e51-a32e-14704cb59c66 2024-11-27 Warnings Exact identifier application number: M013 TYLENOL Extra Strength / TYLENOL Precise Cooling Pain Relief ACETAMINOPHEN, LIDOCAINE, MENTHOL Kenvue Brands LLC 2611e984-0dd5-bda1-e063-6394a90a559a 2024-11-26 Warnings Exact identifier application number: M013 First Aid Only Extra-Strength Non-Aspirin ACETAMINOPHEN Acme United Corporation 6891d57a-10a6-53de-e053-2a91aa0ac7c2 2024-11-26 Warnings Exact identifier application number: M013 Chewable Aspirin ASPIRIN MARC GLASSMAN, INC. c8314910-71ff-5a55-e053-2995a90aafc7 2024-11-26 Warnings Exact identifier application number: M013 Aspirin ASPIRIN Marc Glassman, Inc. 7990ca49-fb30-40fe-9ac4-48e89eac9bb2 2024-11-26 Warnings Exact identifier application number: M013 Enteric Coated Aspirin Regular Strength ASPIRIN Safeway 96359eb6-62bc-4b13-960c-050af99a8c02 2024-11-26 Warnings Exact identifier application number: M013 ASPIRIN Low Dose ASPIRIN Marc Glassman, Inc. 3d519af3-9398-4439-8253-1e5d4612b8e3 2024-11-26 Warnings Exact identifier application number: M013 ACETAMINOPHEN (RED) ACETAMINOPHEN Humanwell PuraCap Pharmaceutical (Wuhan), Ltd. 06eabf4b-f8c0-439a-acf1-aa6e3075c717 2024-11-25 Warnings Exact identifier application number: M013
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 50844-675-03 50844067503 10 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (50844-675-03) 2015-02-03 0000-00-00 Yes No Current 50844-675-26 50844067526 1 BAG in 1 BOX (50844-675-26) / 85000 TABLET, DELAYED RELEASE in 1 BAG 1 bag 2015-02-03 No No Current 50844-675-32 50844067532 120 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (50844-675-32) 2015-02-03 0000-00-00 No No Current