Buffered Aspirin

Product NDC
59779-183
11-digit product format
597790183
Labeler code
59779
Product ID
59779-183_747ba24d-e84b-4a09-8a8d-cd1d0d333df1
Type
HUMAN OTC DRUG
Nonproprietary name
Aspirin
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
CVS Pharmacy
Application
part343
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
1990-03-30
Marketing end
2020-12-29
Substance
ASPIRIN
Active strength
325 mg/1
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct59779-183DDiscontinued by firm2026-10-05
excluded packagepackage59779-18359779-183-30DDiscontinued by firm2026-10-05

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 · 24 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopePackage NDCSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded productproductd630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage59779-183-30d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded productproductf5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage59779-183-30f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-31excluded productproduct2ef7874e63bc…57b86245f4fa…
2025-04-01 02:39 UTC · source 2025-03-31excluded packagepackage59779-183-302ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28excluded productproducta1b67e2a42f9…c4cf2c586c0d…
2025-03-28 20:22 UTC · source 2025-03-28excluded packagepackage59779-183-30a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21excluded productproductcfe11265f3b6…090c488252e2…
2025-03-22 03:12 UTC · source 2025-03-21excluded packagepackage59779-183-30cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10excluded productproductcdf11ea48f46…ba0047e9e063…
2025-03-10 12:48 UTC · source 2025-03-10excluded packagepackage59779-183-30cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31excluded productproduct302b2466d912…e7b80fea0513…
2025-02-02 03:52 UTC · source 2025-01-31excluded packagepackage59779-183-30302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20excluded productproducted331223b511…672a5bd82f5f…
2025-01-20 13:05 UTC · source 2025-01-20excluded packagepackage59779-183-30ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-10excluded productproduct0efc9e666f02…f202fb6c5f17…
2025-01-11 03:41 UTC · source 2025-01-10excluded packagepackage59779-183-300efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-08excluded productproductad56d346431e…cc804d4bbf1e…
2024-11-09 02:27 UTC · source 2024-11-08excluded packagepackage59779-183-30ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03excluded productproduct367a005e9d99…383a685ebd0f…
2024-10-04 04:10 UTC · source 2024-10-03excluded packagepackage59779-183-30367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09excluded productproduct557ba5c1ecfa…9c80585c8c6e…
2024-07-10 04:00 UTC · source 2024-07-09excluded packagepackage59779-183-30557ba5c1ecfa…9c80585c8c6e…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
59779-183-30EA - Each59779-183d3685dc5-6b1b-45a6-813c-b9c1c4b10c6912017-11-06

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ASPIRINACTIVE INGREDIENTR16CO5Y76EBUFFERED ASPIRIN REGULAR STRENGTH (ASPIRIN) TABLET, FILM COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]4
ASPIRINACTIVE MOIETYR16CO5Y76EBUFFERED ASPIRIN REGULAR STRENGTH (ASPIRIN) TABLET, FILM COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]4
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UBUFFERED ASPIRIN REGULAR STRENGTH (ASPIRIN) TABLET, FILM COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]4
CITRIC ACID MONOHYDRATEINACTIVE INGREDIENT2968PHW8QPBUFFERED ASPIRIN REGULAR STRENGTH (ASPIRIN) TABLET, FILM COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]4
DIMETHICONEINACTIVE INGREDIENT92RU3N3Y1OBUFFERED ASPIRIN REGULAR STRENGTH (ASPIRIN) TABLET, FILM COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]4
HYPROMELLOSESINACTIVE INGREDIENT3NXW29V3WOBUFFERED ASPIRIN REGULAR STRENGTH (ASPIRIN) TABLET, FILM COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]4
POLYETHYLENE GLYCOLSINACTIVE INGREDIENT3WJQ0SDW1ABUFFERED ASPIRIN REGULAR STRENGTH (ASPIRIN) TABLET, FILM COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]4
SODIUM LAURYL SULFATEINACTIVE INGREDIENT368GB5141JBUFFERED ASPIRIN REGULAR STRENGTH (ASPIRIN) TABLET, FILM COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]4
TALCINACTIVE INGREDIENT7SEV7J4R1UBUFFERED ASPIRIN REGULAR STRENGTH (ASPIRIN) TABLET, FILM COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]4
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JPBUFFERED ASPIRIN REGULAR STRENGTH (ASPIRIN) TABLET, FILM COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]4