Home NDC 41250-780 Aspirin 81 MG
Product NDC 41250-780
11-digit product format 412500780
Labeler code 41250
Product ID 41250-780_243455d6-158d-31fa-e063-6294a90ad35d
Type HUMAN OTC DRUG
Nonproprietary name ASPIRIN
Dosage form TABLET, DELAYED RELEASE
Route ORAL
Labeler Meijer
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2011-03-01
Marketing end 2026-12-31
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
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 Aspirin 81 MG 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 41250-780-01 Aspirin 81 MG 1 in 1 PACKAGE TABLET, DELAYED RELEASE 1 5 41250-780-01 Aspirin 81 MG 120 in 1 BOTTLE, PLASTIC TABLET, DELAYED RELEASE 120 5 41250-780-06 Aspirin 81 MG 200 in 1 BOTTLE, PLASTIC TABLET, DELAYED RELEASE 200 5 41250-780-06 Aspirin 81 MG 1 in 1 PACKAGE TABLET, DELAYED RELEASE 1 5 41250-780-12 Aspirin 81 MG 300 in 1 BOTTLE, PLASTIC TABLET, DELAYED RELEASE 300 5 41250-780-14 Aspirin 81 MG 32 in 1 BOTTLE, PLASTIC TABLET, DELAYED RELEASE 32 5 41250-780-14 Aspirin 81 MG 1 in 1 PACKAGE TABLET, DELAYED RELEASE 1 5
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded ASPIRIN ACTIVE INGREDIENT R16CO5Y76E ASPIRIN 81 MG (ASPIRIN) TABLET, DELAYED RELEASE [MEIJER] 1 ASPIRIN ACTIVE MOIETY R16CO5Y76E ASPIRIN 81 MG (ASPIRIN) TABLET, DELAYED RELEASE [MEIJER] 1 ANHYDROUS LACTOSE INACTIVE INGREDIENT 3SY5LH9PMK ASPIRIN 81 MG (ASPIRIN) TABLET, DELAYED RELEASE [MEIJER] 1 BROWN IRON OXIDE INACTIVE INGREDIENT 1N032N7MFO ASPIRIN 81 MG (ASPIRIN) TABLET, DELAYED RELEASE [MEIJER] 1 CARNAUBA WAX INACTIVE INGREDIENT R12CBM0EIZ ASPIRIN 81 MG (ASPIRIN) TABLET, DELAYED RELEASE [MEIJER] 1 CELLULOSE, MICROCRYSTALLINE INACTIVE INGREDIENT OP1R32D61U ASPIRIN 81 MG (ASPIRIN) TABLET, DELAYED RELEASE [MEIJER] 1 CROSCARMELLOSE SODIUM INACTIVE INGREDIENT M28OL1HH48 ASPIRIN 81 MG (ASPIRIN) TABLET, DELAYED RELEASE [MEIJER] 1 D&C YELLOW NO. 10 INACTIVE INGREDIENT 35SW5USQ3G ASPIRIN 81 MG (ASPIRIN) TABLET, DELAYED RELEASE [MEIJER] 1 DIACETYLATED MONOGLYCERIDES INACTIVE INGREDIENT 5Z17386USF ASPIRIN 81 MG (ASPIRIN) TABLET, DELAYED RELEASE [MEIJER] 1 DIMETHICONE INACTIVE INGREDIENT 92RU3N3Y1O ASPIRIN 81 MG (ASPIRIN) TABLET, DELAYED RELEASE [MEIJER] 1 HYPROMELLOSE PHTHALATE (24% PHTHALATE, 55 CST) INACTIVE INGREDIENT 87Y6436BKR ASPIRIN 81 MG (ASPIRIN) TABLET, DELAYED RELEASE [MEIJER] 1 HYPROMELLOSES INACTIVE INGREDIENT 3NXW29V3WO ASPIRIN 81 MG (ASPIRIN) TABLET, DELAYED RELEASE [MEIJER] 1 METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1) INACTIVE INGREDIENT 74G4R6TH13 ASPIRIN 81 MG (ASPIRIN) TABLET, DELAYED RELEASE [MEIJER] 1 MINERAL OIL INACTIVE INGREDIENT T5L8T28FGP ASPIRIN 81 MG (ASPIRIN) TABLET, DELAYED RELEASE [MEIJER] 1 POLYETHYLENE GLYCOLS INACTIVE INGREDIENT 3WJQ0SDW1A ASPIRIN 81 MG (ASPIRIN) TABLET, DELAYED RELEASE [MEIJER] 1 POLYSORBATE 80 INACTIVE INGREDIENT 6OZP39ZG8H ASPIRIN 81 MG (ASPIRIN) TABLET, DELAYED RELEASE [MEIJER] 1 SILICON DIOXIDE INACTIVE INGREDIENT ETJ7Z6XBU4 ASPIRIN 81 MG (ASPIRIN) TABLET, DELAYED RELEASE [MEIJER] 1 SODIUM HYDROXIDE INACTIVE INGREDIENT 55X04QC32I ASPIRIN 81 MG (ASPIRIN) TABLET, DELAYED RELEASE [MEIJER] 1 SODIUM LAURYL SULFATE INACTIVE INGREDIENT 368GB5141J ASPIRIN 81 MG (ASPIRIN) TABLET, DELAYED RELEASE [MEIJER] 1 TALC INACTIVE INGREDIENT 7SEV7J4R1U ASPIRIN 81 MG (ASPIRIN) TABLET, DELAYED RELEASE [MEIJER] 1 TITANIUM DIOXIDE INACTIVE INGREDIENT 15FIX9V2JP ASPIRIN 81 MG (ASPIRIN) TABLET, DELAYED RELEASE [MEIJER] 1 TRIETHYL CITRATE INACTIVE INGREDIENT 8Z96QXD6UM ASPIRIN 81 MG (ASPIRIN) TABLET, DELAYED RELEASE [MEIJER] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 41250-780 ASPIRIN 81 MG (ASPIRIN) TABLET, DELAYED RELEASE [MEIJER] 5 Current NDC, Legacy NDC, 7 package rows 20241013_b3e5711c-9529-4eec-871d-de8efa858b86.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 56 of 79 · 1,579 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Publix Fast Relief Effervescent ASPIRIN, CITRIC ACID, SODIUM BICARBONATE Publix Super Markets Inc. 73051f16-2569-7394-e053-2991aa0a5359 2024-11-13 Warnings Exact identifier application number: M013 Quality Choice Effervescent Antacid and Pain Relief ASPIRIN, CITRIC ACID, SODIUM BICARBONATE Chain Drug Marketing Association 70d265de-ff94-e0e4-e053-2a91aa0a962a 2024-11-13 Warnings Exact identifier application number: M013 Quality Choice Extra Strength Effervescent Antacid and Pain Relief ASPIRIN, ANHYDROUS CITRIC ACID, SODIUM BICARBONATE Chain Drug Marketing Association 9f7d0c96-a561-a8a0-e053-2995a90a250b 2024-11-13 Warnings Exact identifier application number: M013 WinCo Foods Effervescent Antacid and Pain Relief ASPIRIN, SODIUM BICARBONATE, CITRIC ACID TABLET WinCo Foods, LLC 0c8a755a-089f-477f-97e9-0dd6fdfbe99d 2024-11-13 Warnings Exact identifier application number: M013 Acetaminophen ACETAMINOPHEN Kroger Company 8fb19444-f0e0-4d26-81e8-6a4b835056d8 2024-11-12 Warnings Exact identifier application number: M013 equate pain reliever ACETAMINOPHEN WALMART INC. 59d01f72-4575-48e2-b914-b6a6456ca7d2 2024-11-11 Warnings Exact identifier application number: M013 pain and fever ACETAMINOPHEN Kroger Company d181560c-1c39-4f2e-8a17-996224ca040f 2024-11-09 Warnings Exact identifier application number: M013 Childrens Tylenol ACETAMINOPHEN Kenvue Brands LLC babcb210-6a47-46ef-b4ea-bdde80411cd3 2024-11-08 Warnings Exact identifier application number: M013 Bayer Genuine Aspirin ASPIRIN Acme United Corporation f7f9dc46-a945-7ae3-e053-6394a90a1192 2024-11-08 Warnings Exact identifier application number: M013 TYLENOL Extra Strength ACETAMINOPHEN Kenvue Brands LLC dd87e342-b0cb-4111-9f15-415dbcda4b77 2024-11-07 Warnings Exact identifier application number: M013 Tylenol Extra Strength ACETAMINOPHEN Kenvue Brands LLC 0c5fdda8-5049-46de-e063-6294a90a592b 2024-11-07 Warnings Exact identifier application number: M013 Childrens TYLENOL ACETAMINOPHEN Kenvue Brands LLC 46ddbfde-54ab-4373-b832-b9c0620b1e9d 2024-11-07 Warnings Exact identifier application number: M013 Childrens TYLENOL ACETAMINOPHEN Kenvue Brands LLC 333f6231-3778-4c1f-9558-2afddca22c86 2024-11-07 Warnings Exact identifier application number: M013 Childrens TYLENOL ACETAMINOPHEN Kenvue Brands LLC 34247a3b-0846-4086-becd-76e630b3b721 2024-11-07 Warnings Exact identifier application number: M013 Childrens TYLENOL ACETAMINOPHEN Kenvue Brands LLC a51c2deb-c703-4dc8-9255-8ac9fe635170 2024-11-07 Warnings Exact identifier application number: M013 Childrens TYLENOL ACETAMINOPHEN Kenvue Brands LLC ce0a1fbc-7345-462b-b0da-c7149bdc288c 2024-11-07 Warnings Exact identifier application number: M013 TYLENOL Extra Strength ACETAMINOPHEN Kenvue Brands LLC 015a6179-bacb-452d-b594-4de628ddc11d 2024-11-07 Warnings Exact identifier application number: M013 TYLENOL Regular Strength ACETAMINOPHEN Kenvue Brands LLC de5c6654-56c5-40d3-a286-f04ed47ac7c8 2024-11-07 Warnings Exact identifier application number: M013 Midol Complete ACETAMINOPHEN, CAFFEINE, AND PYRILAMINE MALEATE Acme United Corporation f7bf126d-a6f1-231a-e053-6294a90a04e1 2024-11-07 Warnings Exact identifier application number: M013 CareOne Childrens Acetaminophen ACETAMINOPHEN American Sales Company 49021ae8-9655-4885-9f74-52df4cdcb26f 2024-11-07 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 41250-780-01 41250078001 1 BOTTLE, PLASTIC in 1 PACKAGE (41250-780-01) > 120 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC 2011-03-01 0000-00-00 No No Current 41250-780-06 41250078006 1 BOTTLE, PLASTIC in 1 PACKAGE (41250-780-06) / 200 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC 2017-12-01 2026-12-31 No No Current 41250-780-12 41250078012 300 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (41250-780-12) 2014-12-01 2026-12-31 No No Current 41250-780-14 41250078014 1 BOTTLE, PLASTIC in 1 PACKAGE (41250-780-14) > 32 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC 2018-07-01 0000-00-00 No No Current