Home NDC 59779-600 Aspirin
Product NDC 59779-600
11-digit product format 597790600
Labeler code 59779
Product ID 59779-600_efb8edcf-a8cc-4d53-bf00-3a5ab8ae67b6
Type HUMAN OTC DRUG
Nonproprietary name Aspirin
Dosage form TABLET, DELAYED RELEASE
Route ORAL
Labeler CVS Pharmacy
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2011-05-01
Marketing end 2028-05-31
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 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 · 60 matching rows.
View current auxiliary records. · View the auxiliary file history.
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
Brand name suffix Enteric Coated 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 59779-600-06 AspirinEnteric Coated 1 in 1 CARTON TABLET, DELAYED RELEASE 1 19 59779-600-06 AspirinEnteric Coated 200 in 1 BOTTLE, PLASTIC TABLET, DELAYED RELEASE 200 19 59779-600-07 AspirinEnteric Coated 1 in 1 CARTON TABLET, DELAYED RELEASE 1 19 59779-600-07 AspirinEnteric Coated 36 in 1 BOTTLE, PLASTIC TABLET, DELAYED RELEASE 36 19 59779-600-14 AspirinEnteric Coated 500 in 1 BOTTLE, PLASTIC TABLET, DELAYED RELEASE 500 19 59779-600-16 AspirinEnteric Coated 1000 in 1 BOTTLE, PLASTIC TABLET, DELAYED RELEASE 1000 19 59779-600-17 AspirinEnteric Coated 300 in 1 BOTTLE, PLASTIC TABLET, DELAYED RELEASE 300 19 59779-600-27 AspirinEnteric Coated 32 in 1 BOTTLE, PLASTIC TABLET, DELAYED RELEASE 32 19 59779-600-27 AspirinEnteric Coated 1 in 1 CARTON TABLET, DELAYED RELEASE 1 19 59779-600-29 AspirinEnteric Coated 150 in 1 BOTTLE, PLASTIC TABLET, DELAYED RELEASE 150 19 59779-600-29 AspirinEnteric Coated 1 in 1 CARTON TABLET, DELAYED RELEASE 1 19 59779-600-32 AspirinEnteric Coated 1 in 1 CARTON TABLET, DELAYED RELEASE 1 19 59779-600-32 AspirinEnteric Coated 120 in 1 BOTTLE, PLASTIC TABLET, DELAYED RELEASE 120 19 59779-600-90 AspirinEnteric Coated 1 in 1 CARTON TABLET, DELAYED RELEASE 1 19 59779-600-90 AspirinEnteric Coated 230 in 1 BOTTLE, PLASTIC TABLET, DELAYED RELEASE 230 19 59779-600-91 AspirinEnteric Coated 360 in 1 BOTTLE TABLET, DELAYED RELEASE 360 19 59779-600-99 AspirinEnteric Coated 2 in 1 CARTON TABLET, DELAYED RELEASE 2 19 59779-600-99 AspirinEnteric Coated 120 in 1 BOTTLE, PLASTIC TABLET, DELAYED RELEASE 120 19
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded ASPIRIN ACTIVE INGREDIENT R16CO5Y76E ASPIRIN ENTERIC COATED (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED] 4 ASPIRIN ACTIVE MOIETY R16CO5Y76E ASPIRIN ENTERIC COATED (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED] 4 CELLULOSE, MICROCRYSTALLINE INACTIVE INGREDIENT OP1R32D61U ASPIRIN ENTERIC COATED (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED] 4 D&C YELLOW NO. 10 INACTIVE INGREDIENT 35SW5USQ3G ASPIRIN ENTERIC COATED (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED] 4 HYPROMELLOSES INACTIVE INGREDIENT 3NXW29V3WO ASPIRIN ENTERIC COATED (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED] 4 METHACRYLIC ACID INACTIVE INGREDIENT 1CS02G8656 ASPIRIN ENTERIC COATED (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED] 4 POLYDEXTROSE INACTIVE INGREDIENT VH2XOU12IE ASPIRIN ENTERIC COATED (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED] 4 POLYETHYLENE GLYCOLS INACTIVE INGREDIENT 3WJQ0SDW1A ASPIRIN ENTERIC COATED (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED] 4 SHELLAC INACTIVE INGREDIENT 46N107B71O ASPIRIN ENTERIC COATED (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED] 4 SODIUM BICARBONATE INACTIVE INGREDIENT 8MDF5V39QO ASPIRIN ENTERIC COATED (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED] 4 SODIUM LAURYL SULFATE INACTIVE INGREDIENT 368GB5141J ASPIRIN ENTERIC COATED (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED] 4 STARCH, CORN INACTIVE INGREDIENT O8232NY3SJ ASPIRIN ENTERIC COATED (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED] 4 TALC INACTIVE INGREDIENT 7SEV7J4R1U ASPIRIN ENTERIC COATED (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED] 4 TITANIUM DIOXIDE INACTIVE INGREDIENT 15FIX9V2JP ASPIRIN ENTERIC COATED (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED] 4 TRIETHYL CITRATE INACTIVE INGREDIENT 8Z96QXD6UM ASPIRIN ENTERIC COATED (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED] 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59779-600 ASPIRIN ENTERIC COATED (ASPIRIN) TABLET, DELAYED RELEASE [CVS PHARMACY] 17 Current NDC, Legacy NDC, 18 package rows 20241116_c55304be-bfc0-46a8-a37e-2e6ba9098394.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 22 of 79 · 1,579 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join TYLENOL Regular Strength ACETAMINOPHEN Kenvue Brands LLC 01f41fae-4abb-4b96-ab09-a7d3dfc286cd 2026-01-26 Warnings Exact identifier application number: M013 pain relief ACETAMINOPHEN Meijer Distribution Inc ec4dbb71-b507-42a3-9b68-14d4b6621ec1 2026-01-23 Warnings Exact identifier application number: M013 Adult Low Dose Aspirin ASPIRIN NCS HealthCare of KY, LLC dba Vangard Labs 9105eff0-1c22-4298-8ee5-9fb7a1de12f1 2026-01-23 Warnings Exact identifier application number: M013 Extra Strength Pain Relief ACETAMINOPHEN Preferred Pharmaceuticals Inc. c70e3b8e-071d-4b9a-9393-ad8aa09c6b6e 2026-01-22 Warnings Exact identifier application number: M013 Tylenol Extra Strength ACETAMINOPHEN Kenvue Brands LLC 17cfa99d-abb2-4d77-9e0e-e77109fbb61a 2026-01-21 Warnings Exact identifier application number: M013 Dr Simi Extra Strength Acetaminophen 250 mg, Aspirin 250 mg, and Caffeine 65 mg ACETAMINOPHEN 250 MG, ASPIRIN 250 MG, AND CAFFEINE 65 MG Farmacias De Similares TX LLC 48ea0a2c-511b-4805-e063-6394a90a1225 2026-01-21 Warnings Exact identifier application number: M013 childrens mapap ACETAMINOPHEN Major Pharmaceuticals a1b0ccf0-cf24-4b34-b42a-aa1cc1e57f60 2026-01-20 Warnings Exact identifier application number: M013 EXTRA STRENGTH ACETAMINOPHEN ACETAMINOPHEN WALGREENS CO. 9b756e4e-6c56-43aa-a5bc-5b649440e759 2026-01-20 Warnings Exact identifier application number: M013 EXTRA STRENGTH PAIN RELIEVER PM ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE WALGREENS CO. 5a58d620-a0ec-48d7-92dd-3f3f78ec10ea 2026-01-20 Warnings Exact identifier application number: M013 equate pain reliever ACETAMINOPHEN Wal-Mart Stores Inc d4e438c6-80dd-4531-91e6-bc4ca7a8570f 2026-01-20 Warnings Exact identifier application number: M013 Unishield Extra Strength Non-Aspirin ACETAMINOPHEN Unishield ba0ec1eb-db85-6a7f-e053-2995a90aafe5 2026-01-19 Warnings Exact identifier application number: M013 pain relief ACETAMINOPHEN HyVee Inc 24acd62f-72b1-418a-b733-7e4888f3c0a3 2026-01-16 Warnings Exact identifier application number: M013 Acetaminophen Extra Strength ACETAMINOPHEN Cardinal Health 110, LLC. DBA Leader dd8b13a5-07df-4cec-92c3-1a662b1e1a56 2026-01-16 Warnings Exact identifier application number: M013 EXTRA STRENGTH HEADACHE RELIEF ACETAMINOPHEN, ASPIRIN, CAFFEINE WALGREENS 7d8f8389-730d-494e-a0af-5a91a3c99e17 2026-01-16 Warnings Exact identifier application number: M013 TENSION HEADACHE RELIEF ACETAMINOPHEN AND CAFFEINE WALGREENS 54aff6a0-2778-472f-90ba-375d6bce6ee8 2026-01-16 Warnings Exact identifier application number: M013 EXTRA STRENGTH HEADACHE RELIEF ACETAMINOPHEN, ASPIRIN, CAFFEINE WALGREENS 097fbab7-3886-4e75-b037-f03adcf3859f 2026-01-16 Warnings Exact identifier application number: M013 Pain Reliever ACETAMINOPHEN WALGREENS CO. bdb09e15-8e17-4987-99d0-bab8856a2109 2026-01-16 Warnings Exact identifier application number: M013 acetaminophen ACETAMINOPHEN HF Acquisition Co LLC, DBA HealthFirst 4870ff00-f727-814d-e063-6394a90a6c8e 2026-01-15 Warnings Exact identifier application number: M013 Aspirin ASPIRIN HyVee Inc 957b13a4-4086-459f-8fa0-9708b317fabe 2026-01-15 Warnings Exact identifier application number: M013 Unisom PM Pain Nighttime Sleep Aid and Pain Reliever ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE Chattem, Inc. 451daeeb-88a9-44b1-9a2d-1ff0b0ec41cb 2026-01-14 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 59779-600-06 59779060006 1 BOTTLE, PLASTIC in 1 CARTON (59779-600-06) / 200 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC 2011-05-01 2027-12-31 No No Current 59779-600-07 59779060007 1 in 1 CARTON Historical 59779-600-14 59779060014 500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (59779-600-14) 2011-05-01 2028-05-31 No No Current 59779-600-16 59779060016 1000 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (59779-600-16) 2011-05-01 2028-05-31 No No Current 59779-600-17 59779060017 300 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (59779-600-17) 2011-05-01 2028-05-31 No No Current 59779-600-27 59779060027 1 BOTTLE, PLASTIC in 1 CARTON (59779-600-27) / 32 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC 2011-05-01 2027-04-30 No No Current 59779-600-29 59779060029 150 in 1 BOTTLE, PLASTIC Historical 59779-600-32 59779060032 1 BOTTLE, PLASTIC in 1 CARTON (59779-600-32) / 120 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC 2011-05-01 2028-05-31 No No Current 59779-600-90 59779060090 1 BOTTLE, PLASTIC in 1 CARTON (59779-600-90) > 230 TABLET, COATED in 1 BOTTLE, PLASTIC 2011-05-01 0000-00-00 No No Current 59779-600-91 59779060091 360 TABLET, COATED in 1 BOTTLE (59779-600-91) 2011-05-01 0000-00-00 No No Current 59779-600-99 59779060099 2 in 1 CARTON Historical