aspirin

Product NDC
56062-416
Requested package NDC
56062-416-78
11-digit product format
560620416
Labeler code
56062
Product ID
56062-416_458a5aee-4aea-4dc3-aa88-3f1cf2e5b47f
Type
HUMAN OTC DRUG
Nonproprietary name
Aspirin
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Publix Super Markets Inc
Application
part343
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
1988-09-15
Marketing end
0000-00-00
Substance
ASPIRIN
Active strength
325 mg/1
NDC exclude flag
No
Listing certified through
2020-12-31
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 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage56062-41656062-416-78DDiscontinued 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 · 9 matching rows.

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

Captured / source date, Snapshot, Source SHA-256 table
Captured / source dateSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-312ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-100efc9e666f02…f202fb6c5f17…

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
56062-416-78EA - Each56062-416c9de225f-df02-4a5c-92bd-a0e8dc986a3812022-06-06
56062-416-87EA - Each56062-4163b0d4c27-3670-4f7d-a097-df14e004df6712013-02-13

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ASPIRINACTIVE INGREDIENTR16CO5Y76EASPIRIN TABLET [PUBLIX SUPER MARKETS INC]2
ASPIRINACTIVE MOIETYR16CO5Y76EASPIRIN TABLET [PUBLIX SUPER MARKETS INC]2
CALCIUM PHOSPHATE, DIBASIC, DIHYDRATEINACTIVE INGREDIENTO7TSZ97GEPASPIRIN TABLET [PUBLIX SUPER MARKETS INC]2
HYPROMELLOSESINACTIVE INGREDIENT3NXW29V3WOASPIRIN TABLET [PUBLIX SUPER MARKETS INC]2
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJASPIRIN TABLET [PUBLIX SUPER MARKETS INC]2
TALCINACTIVE INGREDIENT7SEV7J4R1UASPIRIN TABLET [PUBLIX SUPER MARKETS INC]2
TRIACETININACTIVE INGREDIENTXHX3C3X673ASPIRIN TABLET [PUBLIX SUPER MARKETS INC]2

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
56062-416-7856062041678100 TABLET, FILM COATED in 1 BOTTLE (56062-416-78) 1988-09-150000-00-00NoNoCurrent