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 43 of 79 · 1,570 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join equate childrens pain and fever ACETAMINOPHEN Wal-Mart Stores Inc f15037a5-4e43-4dd6-93b8-b37a1cc22cd6 2025-07-07 Warnings Exact identifier application number: M013 Childrens Acetaminophen Oral Liquid Grape Flavor ACETAMINOPHEN AARNA USA INC. 39347f5d-2d3c-0c23-e063-6294a90a3a46 2025-07-05 Warnings Exact identifier application number: M013 Childrens Pain and Fever ACETAMINOPHEN Meijer Distribution Inc be841460-98b4-4448-a494-09ff161fd131 2025-07-02 Warnings Exact identifier application number: M013 Adult Low Dose Aspirin ASPIRIN Advanced Rx LLC ad0d6a5c-eee9-406c-8d7f-1df9b45f5340 2025-07-02 Warnings Exact identifier application number: M013 EXTRA STRENGHT HEADACHE RELIEF ACETAMINOPHEN, ASPIRIN, CAFFEINE Lil' Drug Store Products, Inc. ec04eb5d-96c0-ddb4-e053-2a95a90a4a92 2025-07-02 Warnings Exact identifier application number: M013 Maximum Strength Cough and Chest Congestion and Nighttime Severe Cold and Flu Combo pack DEXTROMETHORPHAN HBR, GUAIFENESIN, ACETAMINOPHEN, DOXYLAMINE SUCCINATE Genexa Inc. 18835205-a9e3-15c2-e063-6394a90a8107 2025-07-02 Warnings Exact identifier application number: M013 FeverAll ACETAMINOPHEN Sun Pharmaceutical Industries, Inc. 8970b91b-5f3c-4764-9e23-25dcb398d0a7 2025-07-02 Warnings Exact identifier application number: M013 Childrens Pain and Fever ACETAMINOPHEN Meijer Distribution Inc 11c9712d-c3b2-49cd-9c2b-0f57190c954e 2025-07-02 Warnings Exact identifier application number: M013 Aspirin Regular Strength ASPIRIN United Natural Foods, Inc. dba UNFI 979973c1-661a-4384-8b92-fd901ebde558 2025-07-01 Warnings Exact identifier application number: M013 Pain and Fever Childrens ACETAMINOPHEN CVS Pharmacy f6bbce1c-9790-4ca4-847f-579c594ffe0b 2025-07-01 Warnings Exact identifier application number: M013 Pain Reliever ACETAMINOPHEN WALGREENS 07d2e322-2465-79e5-e063-6294a90a5ea4 2025-06-30 Warnings Exact identifier application number: M013 Pain Relief ACETAMINOPHEN DISCOUNT DRUG MART 66c0cf26-357b-4722-9100-3b86d507a8cd 2025-06-30 Warnings Exact identifier application number: M013 ALLERGY DIPHENHYDRAMINE HYDROCHLORIDE Kroger Company bc019c9e-8fac-5fd3-e053-2a95a90a7ccd 2025-06-25 Warnings Exact identifier application number: M013 ACETAMINOPHEN Extra Strength ACETAMINOPHEN TIME CAP LABS INC fd24d0e0-4f36-42d3-9149-2fb957690305 2025-06-25 Warnings Exact identifier application number: M013 Aspirin Low Dose ASPIRIN ATLANTIC BIOLOGICALS CORP. 024c5054-959f-4ea5-a71f-c0e16cc4b90c 2025-06-24 Warnings Exact identifier application number: M013 CHILDRENS ACETAMINOPHEN CHILDRENS ACETAMINOPHEN ORAL AARNA USA INC. 38070d15-2678-4e59-e063-6294a90ab690 2025-06-20 Warnings Exact identifier application number: M013 TYLENOL Extra Strength ACETAMINOPHEN Morning Star OTC 8502ea21-937d-4b33-a3e0-ffab5dc38cd8 2025-06-19 Warnings Exact identifier application number: M013 Tylenol PM Extra Strength ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE Morning Star OTC 6cd07a01-7034-4994-bbd3-bedcdf7d5b83 2025-06-19 Warnings Exact identifier application number: M013 DRX CHOICE Tension Headache ACETAMINOPHEN, CAFFEINE Raritan Pharmaceuticals Inc. 8a5cb38b-669d-4177-b33b-d73c7ef48d18 2025-06-13 Warnings Exact identifier application number: M013 good sense childrens pain and fever ACETAMINOPHEN NuCare Pharmaceuticals,Inc. 3777f4fb-d279-199d-e063-6394a90acf36 2025-06-13 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