Home NDC 55910-600 Aspirin 81 mg
Product NDC 55910-600
11-digit product format 559100600
Labeler code 55910
Product ID 55910-600_15dd3324-0cca-45d0-8c73-794a6027ae5d
Type HUMAN OTC DRUG
Nonproprietary name Aspirin
Dosage form TABLET, DELAYED RELEASE
Route ORAL
Labeler DOLGENCORP, LLC
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2011-05-01
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 2027-12-31
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 · 12 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 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 81 mg
Listing expiration 2027-12-31 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 · 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 55910-600-32 Aspirin 81 mg 120 in 1 BOTTLE, PLASTIC TABLET, DELAYED RELEASE 120 24 55910-600-32 Aspirin 81 mg 1 in 1 CARTON TABLET, DELAYED RELEASE 1 24 55910-600-69 Aspirin 81 mg 1 in 1 CARTON TABLET, DELAYED RELEASE 1 24 55910-600-69 Aspirin 81 mg 144 in 1 BOTTLE TABLET, DELAYED RELEASE 144 24
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded ASPIRIN ACTIVE INGREDIENT R16CO5Y76E ASPIRIN 81 MG (ASPIRIN) TABLET, COATED [DOLGENCORP, LLC] 10 ASPIRIN ACTIVE MOIETY R16CO5Y76E ASPIRIN 81 MG (ASPIRIN) TABLET, COATED [DOLGENCORP, LLC] 10 CELLULOSE, MICROCRYSTALLINE INACTIVE INGREDIENT OP1R32D61U ASPIRIN 81 MG (ASPIRIN) TABLET, COATED [DOLGENCORP, LLC] 10 D&C YELLOW NO. 10 INACTIVE INGREDIENT 35SW5USQ3G ASPIRIN 81 MG (ASPIRIN) TABLET, COATED [DOLGENCORP, LLC] 10 FD&C YELLOW NO. 6 INACTIVE INGREDIENT H77VEI93A8 ASPIRIN 81 MG (ASPIRIN) TABLET, COATED [DOLGENCORP, LLC] 10 FERROSOFERRIC OXIDE INACTIVE INGREDIENT XM0M87F357 ASPIRIN 81 MG (ASPIRIN) TABLET, COATED [DOLGENCORP, LLC] 10 HYPROMELLOSES INACTIVE INGREDIENT 3NXW29V3WO ASPIRIN 81 MG (ASPIRIN) TABLET, COATED [DOLGENCORP, LLC] 10 POLYDEXTROSE INACTIVE INGREDIENT VH2XOU12IE ASPIRIN 81 MG (ASPIRIN) TABLET, COATED [DOLGENCORP, LLC] 10 POLYETHYLENE GLYCOLS INACTIVE INGREDIENT 3WJQ0SDW1A ASPIRIN 81 MG (ASPIRIN) TABLET, COATED [DOLGENCORP, LLC] 10 PROPYLENE GLYCOL INACTIVE INGREDIENT 6DC9Q167V3 ASPIRIN 81 MG (ASPIRIN) TABLET, COATED [DOLGENCORP, LLC] 10 SILICON DIOXIDE INACTIVE INGREDIENT ETJ7Z6XBU4 ASPIRIN 81 MG (ASPIRIN) TABLET, COATED [DOLGENCORP, LLC] 10 SODIUM BICARBONATE INACTIVE INGREDIENT 8MDF5V39QO ASPIRIN 81 MG (ASPIRIN) TABLET, COATED [DOLGENCORP, LLC] 10 TITANIUM DIOXIDE INACTIVE INGREDIENT 15FIX9V2JP ASPIRIN 81 MG (ASPIRIN) TABLET, COATED [DOLGENCORP, LLC] 10 TRIACETIN INACTIVE INGREDIENT XHX3C3X673 ASPIRIN 81 MG (ASPIRIN) TABLET, COATED [DOLGENCORP, LLC] 10 TRIETHYL CITRATE INACTIVE INGREDIENT 8Z96QXD6UM ASPIRIN 81 MG (ASPIRIN) TABLET, COATED [DOLGENCORP, LLC] 10
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 55910-600 ASPIRIN 81 MG (ASPIRIN) TABLET, DELAYED RELEASE [DOLGENCORP, LLC] 22 Current NDC, Legacy NDC, 4 package rows 20240825_b4064039-2345-4227-b83d-54dc13a838d3.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 51 of 79 · 1,570 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join ACETAMINOPHEN ACETAMINOPHEN CHAIN DRUG MARKETING ASSOCIATION INC a3031139-4709-43f2-95a8-89840c595f7f 2024-12-26 Warnings Exact identifier application number: M013 Acetaminophen 250mg Aspirin 250mg Caffeine 65mg ACETAMINOPHEN 250MG ASPIRIN 250MG CAFFEINE 65MG WALGREENS CO. 98bb28ed-d146-ca3d-e053-2a95a90a9eaf 2024-12-26 Warnings Exact identifier application number: M013 Acetaminophen 500mg Caffeine 60mg Pyrilamine maleate 15mg ACETAMINOPHEN 500MG CAFFEINE 60MG PYRILAMINE MALEATE 15MG WALGREENS CO. 982faa74-d498-cd1e-e053-2995a90afa1e 2024-12-25 Warnings Exact identifier application number: M013 Childrens Pain and Fever ACETAMINOPHEN AptaPharma Inc. 11bf6e1b-aed9-4f8f-9f03-ea911ae9f702 2024-12-23 Warnings Exact identifier application number: M013 Rugby Regular Strength Acetaminophen ACETAMINOPHEN RUGBY LABORATORIES 295b0d00-4d4a-405f-9325-d01c5d4f3ed4 2024-12-20 Warnings Exact identifier application number: M013 Walgreens Pain Relief Powder ASPIRIN AND CAFFEINE Walgreens Co. 61493d34-2432-4683-9b32-e1851a4337be 2024-12-18 Warnings Exact identifier application number: M013 Reese Headache Powders ASPIRIN AND CAFFEINE Reese Pharmaceutical Co 386f7a6c-4bfc-4140-a67b-07f6b520d58f 2024-12-18 Warnings Exact identifier application number: M013 NobleAid PAIN RELIEVER ASPIRIN Noble Otc LLC aa08e488-2f69-4d7e-86ba-ccfad563edcf 2024-12-18 Warnings Exact identifier application number: M013 Dollar General Headache Powders ASPIRIN AND CAFFEINE Dolgencorp, LLC 11b0271b-d65c-49c4-a081-d71044a0e04c 2024-12-18 Warnings Exact identifier application number: M013 Family Wellness Pain Relief Powder ASPIRIN AND CAFFEINE Family Dollar Services Inc b2e55de7-3c36-49cc-8f7f-1013fd1ec359 2024-12-18 Warnings Exact identifier application number: M013 Best Choice Pain Relief Powder ASPIRIN AND CAFFEINE Value Merch a95b9b22-ea5c-4a02-b35d-c8ae1e117604 2024-12-18 Warnings Exact identifier application number: M013 Walmart Pain Relief Powder ASPIRIN AND CAFFEINE Walmart c69aa61f-6a74-40a3-8737-195fa545e261 2024-12-18 Warnings Exact identifier application number: M013 Quality Choice Pain Relief Powder ASPIRIN AND CAFFEINE Chain Drug Marketing Association 8e1f4057-4968-4523-9b3f-55aea421b674 2024-12-18 Warnings Exact identifier application number: M013 Equaline Effervescent Antacid and Pain Relief ASPIRIN, CITRIC ACID, SODIUM BICARBONATE United Natural Foods, Inc. dba UNFI 739237a5-cc62-8ad6-e053-2991aa0a91f8 2024-12-17 Warnings Exact identifier application number: M013 NOTTS - Muscle Aches and Pain ACETAMINOPHEN VIVUNT PHARMA LLC e6741300-4573-2580-e053-2a95a90a599c 2024-12-17 Warnings Exact identifier application number: M013 Extra Strength Pain Reliever, Caseys 4good ACETAMINOPHEN 500MG, FILM-COATED CAPLET Lil' Drug Store Products, Inc. e5fc5340-c224-e02b-e053-2a95a90a5297 2024-12-16 Warnings Exact identifier application number: M013 Pain Reliever, Caseys 4good ACETAMINOPHEN 500 MG, TABLET Lil' Drug Store Products, Inc. 039d2cf1-57f6-4d9d-e063-6394a90a5492 2024-12-16 Warnings Exact identifier application number: M013 Extra Strength Headache, Caseys 4good ACETAMINOPHEN, ASPIRIN, CAFFEINE TABLET Lil' Drug Store Products, Inc. 0425c6a8-a3ea-24ad-e063-6294a90ae15a 2024-12-16 Warnings Exact identifier application number: M013 Lil Drug Store Childrens Pain and Fever ACETAMINOPHEN Lil' Drug Store Products, Inc. 5fcd41ad-449f-4090-be19-eae4171de891 2024-12-16 Warnings Exact identifier application number: M013 Acetaminophen 250mg Aspirin 250mg Caffeine 65mg ACETAMINOPHEN 250MG ASPIRIN 250MG CAFFEINE 65MG CVS Pharmacy b9e75551-1e50-9896-e053-2a95a90aafd4 2024-12-14 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 55910-600-32 55910060032 1 BOTTLE, PLASTIC in 1 CARTON (55910-600-32) / 120 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC 2011-05-01 0000-00-00 No No Current 55910-600-69 55910060069 1 BOTTLE in 1 CARTON (55910-600-69) > 144 TABLET, COATED in 1 BOTTLE 1 bottle 2011-05-01 0000-00-00 No No Current