Home NDC 41250-780-01 Aspirin 81 MG
Product NDC 41250-780
Requested package NDC 41250-780-01
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 72 of 79 · 1,576 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Excedrin Tension Headache ACETAMINOPHEN, CAFFEINE Haleon US Holdings LLC 12c074d1-81ac-47d2-8747-b018cda0058a 2024-03-13 Warnings Exact identifier application number: M013 Menstrual Complete ACETAMINOPHEN, CAFFEINE, PYRILAMINE MALEATE Strive Pharmaceuticals Inc. 78c12459-3b27-4ed0-943d-520794eb438d 2024-03-07 Warnings Exact identifier application number: M013 Pain Reliever fever Reducer Extra Strength ACETAMINOPHEN CVS Pharmacy 7b5263ad-01b7-4fc5-9384-4da8efe89e35 2024-03-06 Warnings Exact identifier application number: M013 Excedrin Extra Strength Geltabs ACETAMINOPHEN, ASPRIN, CAFFEINE Haleon US Holdings LLC 11a8439b-0159-4351-b0f5-fe7fad6a33c0 2024-03-05 Warnings Exact identifier application number: M013 Winco Foods Effervescent Pain Relief ASPIRIN Winco Foods, LLC 128afdd7-a9d1-8957-e063-6294a90af569 2024-03-05 Warnings Exact identifier application number: M013 Aspirin Low Dose Safety Coated ASPIRIN Care One (Retail Business Services, LLC.) 6659e103-fa03-4de0-af42-d2fbd548a87c 2024-03-05 Warnings Exact identifier application number: M013 Dolex Children Pain and Fever ACETAMINOPHEN Pharmadel LLC f9158463-aeb1-5de0-e053-6294a90a748b 2024-03-04 Warnings Exact identifier application number: M013 SEDALMEX FORTE ACETAMINOPHEN, ASPIRIN, CAFFEINE Belmora LLC 33b3508e-4caa-4d05-9b15-cb82a2ee2d4d 2024-02-28 Warnings Exact identifier application number: M013 Pain Relief ACETAMINOPHEN AMERISOURCE BERGEN 2b923a97-836c-4dac-a8c0-3047a35fb62e 2024-02-23 Warnings Exact identifier application number: M013 Pain Reliever PM Extra Strength ACETAMINOPHEN, DIPHENHYDRAMINE HCL BJWC (Berkley & Jensen / BJ's) b20a08f3-c9c0-4bd9-8ce0-acb932b5bb86 2024-02-22 Warnings Exact identifier application number: M013 M-PAP ACETAMINOPHEN Bryant Ranch Prepack 31a41976-7f65-42d7-acf5-de9c2c5ca58e 2024-02-20 Warnings Exact identifier application number: M013 Publix Fast Relief Effervescent - Original Flavor ASPIRIN PUBLIX SUPER MARKETS INC. 0a342f72-45fd-3e12-e063-6394a90ae33e 2024-02-16 Warnings Exact identifier application number: M013 Equaline Effervescent Pain Reliever ASPIRIN UNITED NATURAL FOODS, INC. DBA UNFI 0761299a-e913-7665-e063-6394a90a6003 2024-02-16 Warnings Exact identifier application number: M013 TopCare Effervescent Pain Relief ASPIRIN TOPCO ASSOCIATES LLC 075f36e1-110c-e839-e063-6294a90a89d7 2024-02-16 Warnings Exact identifier application number: M013 Extra Strength Pain Reliever ACETAMINOPHEN INGLES MARKETS, INC. 115d0b4f-6f0f-79a9-e063-6394a90ab18a 2024-02-14 Warnings Exact identifier application number: M013 PANADOL ACETAMINOPHEN Haleon US Holdings LLC e1799765-c247-42b4-ad6a-8ba7d136abf2 2024-02-06 Warnings Exact identifier application number: M013 Panadol Cold and Flu NonDrowsy ACETAMINOPHEN AND PHENYLEPRINE HCL Haleon US Holdings LLC f626ab17-01c9-4493-ba9e-0c8c11146384 2024-02-06 Warnings Exact identifier application number: M013 PANADOL Extra ACETAMINOPHEN AND CAFFEINE Haleon US Holdings LLC e5c2d88a-d903-4ca0-b895-f27e791dfc4e 2024-02-06 Warnings Exact identifier application number: M013 PANADOL Extra Strength ACETAMINOPHEN Haleon US Holdings LLC b2fe7f47-1a2e-40ee-8f8f-38f2028dce1b 2024-02-06 Warnings Exact identifier application number: M013 PANADOL Extra Strength ACETAMINOPHEN Haleon US Holdings LLC 9d384e88-5c11-4600-ac6c-a38371570138 2024-02-06 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