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 76 of 79 · 1,576 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Acetaminophen Extra Strength ACETAMINOPHEN Aurohealth LLC 03d42892-4465-4089-90a7-cd5f00c35602 2023-11-29 Warnings Exact identifier application number: M013 Acetaminophen Extra Strength ACETAMINOPHEN Aurohealth LLC 57bb1acc-b9a0-48cd-8e5c-33712441ce81 2023-11-29 Warnings Exact identifier application number: M013 Acetaminophen Regular Strength ACETAMINOPHEN Aurohealth LLC cc0ab7a1-e535-4dc8-962f-c58949fc1737 2023-11-29 Warnings Exact identifier application number: M013 Acetaminophen ACETAMINOPHEN Aurohealth LLC a4ff94b9-c248-4cd3-8491-38e9555cc22e 2023-11-29 Warnings Exact identifier application number: M013 Aurophen Extra Strength for Adults ACETAMINOPHEN Aurohealth LLC d59c5f04-4bcc-4a52-a42f-e049506f00de 2023-11-29 Warnings Exact identifier application number: M013 Aurophen Extra Strength for Adults ACETAMINOPHEN Aurohealth LLC a769094b-1e91-4ca7-ba67-21aa7e312910 2023-11-29 Warnings Exact identifier application number: M013 Acetaminophen ACETAMINOPHEN Aurohealth LLC 30756257-f748-4a5d-b031-dd267d0f91ad 2023-11-29 Warnings Exact identifier application number: M013 Aurophen Regular Strength ACETAMINOPHEN Aurohealth LLC 8eda893f-5266-4b7a-95b9-2e194973cf06 2023-11-29 Warnings Exact identifier application number: M013 Childrens Pain Relief ACETAMINOPHEN Aurohealth LLC 00ec6518-b5e3-49d1-a342-139381c3bfd2 2023-11-29 Warnings Exact identifier application number: M013 CHILDRENS PAIN RELIEF ACETAMINOPHEN Better Living Brands, LLC fadb4c09-071f-56c0-e053-6294a90ae6c1 2023-11-28 Warnings Exact identifier application number: M013 Acetaminophen and Diphenhydramine hydrochloride ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE Better Living Brands, LLC fc07d516-9ffe-9989-e053-6294a90ae1a5 2023-11-28 Warnings Exact identifier application number: M013 NOTTS - Tension Headache ACETAMINOPHEN, CAFFEINE VIVUNT PHARMA LLC 08f2ae03-967b-ad7e-e063-6294a90a8484 2023-11-24 Warnings Exact identifier application number: M013 Sanatos Multi Symptoms Nighttime ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE Pharmadel LLC 0a60326a-a17b-e843-e063-6394a90ac211 2023-11-22 Warnings Exact identifier application number: M013 Sanatos Nighttime Multi Symptoms ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE Pharmadel LLC 0ab188f3-f7f9-d665-e063-6294a90a198a 2023-11-22 Warnings Exact identifier application number: M013 ASPIRIN ASPIRIN TIME CAP LABS INC fe12519c-3e5f-4592-bd34-2d6b81b981f4 2023-11-22 Warnings Exact identifier application number: M013 Rugby Regular Strength Acetaminophen ACETAMINOPHEN A-S Medication Solutions 400d4a29-9e39-4e74-8272-37be5d789924 2023-11-22 Warnings Exact identifier application number: M013 RIGHT REMEDIES Pain Relief Extra Strength Caplet ACETAMINOPHEN Strive Pharmaceuticals Inc. dcce28d9-8528-489e-b995-1d98e9d0e6ad 2023-11-21 Warnings Exact identifier application number: M013 Sanatos Multi Symptom Daytime ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCI Pharmadel LLC 0ab11691-5b29-55fc-e063-6394a90aa328 2023-11-17 Warnings Exact identifier application number: M013 Acetaminophen ACETAMINOPHEN A-S Medication Solutions 1e223faa-f6d0-4235-bc4c-6cfca84a5b0a 2023-11-17 Warnings Exact identifier application number: M013 SanaTos X ACETAMINOPHEN, DEXTROMETHORPHAN HBR,GUAIFENESIN, PHENYLEPHRINE HCI Pharmadel LLC 85b8ef3d-7318-7f3b-e053-2991aa0a0777 2023-11-14 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