Home NDC 59779-945 ASPIRIN
Product NDC 59779-945
11-digit product format 597790945
Labeler code 59779
Product ID 59779-945_306e0e90-2dfe-4b85-8ddf-c3b2ae09035b
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 2014-07-25
Marketing end 2027-05-31
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 · 25 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 Low Strength 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 59779-945-07 ASPIRINLow Strength 36 in 1 BOTTLE TABLET, DELAYED RELEASE 36 18 59779-945-07 ASPIRINLow Strength 1 in 1 CARTON TABLET, DELAYED RELEASE 1 18 59779-945-17 ASPIRINLow Strength 300 in 1 BOTTLE TABLET, DELAYED RELEASE 300 18 59779-945-17 ASPIRINLow Strength 1 in 1 CARTON TABLET, DELAYED RELEASE 1 18 59779-945-32 ASPIRINLow Strength 1 in 1 CARTON TABLET, DELAYED RELEASE 1 18 59779-945-32 ASPIRINLow Strength 120 in 1 BOTTLE, PLASTIC TABLET, DELAYED RELEASE 120 18 59779-945-51 ASPIRINLow Strength 365 in 1 BOTTLE, PLASTIC TABLET, DELAYED RELEASE 365 18
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded ASPIRIN ACTIVE INGREDIENT R16CO5Y76E ASPIRIN LOW STRENGTH (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED] 3 ASPIRIN ACTIVE MOIETY R16CO5Y76E ASPIRIN LOW STRENGTH (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED] 3 CELLULOSE, MICROCRYSTALLINE INACTIVE INGREDIENT OP1R32D61U ASPIRIN LOW STRENGTH (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED] 3 FD&C RED NO. 40 INACTIVE INGREDIENT WZB9127XOA ASPIRIN LOW STRENGTH (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED] 3 FD&C YELLOW NO. 6 INACTIVE INGREDIENT H77VEI93A8 ASPIRIN LOW STRENGTH (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED] 3 HYPROMELLOSES INACTIVE INGREDIENT 3NXW29V3WO ASPIRIN LOW STRENGTH (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED] 3 METHACRYLIC ACID INACTIVE INGREDIENT 1CS02G8656 ASPIRIN LOW STRENGTH (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED] 3 POLYDEXTROSE INACTIVE INGREDIENT VH2XOU12IE ASPIRIN LOW STRENGTH (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED] 3 POLYETHYLENE GLYCOLS INACTIVE INGREDIENT 3WJQ0SDW1A ASPIRIN LOW STRENGTH (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED] 3 SHELLAC INACTIVE INGREDIENT 46N107B71O ASPIRIN LOW STRENGTH (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED] 3 SODIUM BICARBONATE INACTIVE INGREDIENT 8MDF5V39QO ASPIRIN LOW STRENGTH (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED] 3 SODIUM LAURYL SULFATE INACTIVE INGREDIENT 368GB5141J ASPIRIN LOW STRENGTH (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED] 3 STARCH, CORN INACTIVE INGREDIENT O8232NY3SJ ASPIRIN LOW STRENGTH (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED] 3 TALC INACTIVE INGREDIENT 7SEV7J4R1U ASPIRIN LOW STRENGTH (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED] 3 TITANIUM DIOXIDE INACTIVE INGREDIENT 15FIX9V2JP ASPIRIN LOW STRENGTH (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED] 3 TRIACETIN INACTIVE INGREDIENT XHX3C3X673 ASPIRIN LOW STRENGTH (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED] 3 TRIETHYL CITRATE INACTIVE INGREDIENT 8Z96QXD6UM ASPIRIN LOW STRENGTH (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED] 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59779-945 ASPIRIN LOW STRENGTH (ASPIRIN) TABLET, DELAYED RELEASE [CVS PHARMACY] 16 Current NDC, Legacy NDC, 7 package rows 20240718_6e1c1129-562b-4a8a-ac37-db3cb2a82735.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 1 of 83 · 1,657 matching rows.
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 59779-945-07 59779094507 36 in 1 BOTTLE Historical 59779-945-17 59779094517 300 in 1 BOTTLE Historical 59779-945-32 59779094532 1 BOTTLE, PLASTIC in 1 CARTON (59779-945-32) > 120 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC 2014-07-25 0000-00-00 No No Current 59779-945-51 59779094551 365 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (59779-945-51) 2014-07-25 2027-05-31 No No Current