FDA.reportPublic FDA data

pain relief

Product NDC
59779-484
Requested package NDC
59779-484-90
11-digit product format
597790484
Labeler code
59779
Product ID
59779-484_e5a306c3-d3d7-4189-8be4-53ab2354582b
Type
HUMAN OTC DRUG
Nonproprietary name
Acetaminophen
Dosage form
TABLET
Route
ORAL
Labeler
CVS Pharmacy
Application
part343
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
1991-07-15
Marketing end
0000-00-00
Substance
ACETAMINOPHEN
Active strength
500 mg/1
NDC exclude flag
No
Listing certified through
2023-12-31
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 packagepackage59779-48459779-484-90DDiscontinued 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 · 12 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…
2024-11-09 02:27 UTC · source 2024-11-08ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09557ba5c1ecfa…9c80585c8c6e…

Reported adverse events (FAERS/openFDA)#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDCEffectiveRelated label
59779-484-022024-08-14CVS Pharmacy, Inc. Pain Relief Drug Facts
59779-484-472024-08-14CVS Pharmacy, Inc. Pain Relief Drug Facts
59779-484-522024-08-14CVS Pharmacy, Inc. Pain Relief Drug Facts
59779-484-622024-08-14CVS Pharmacy, Inc. Pain Relief Drug Facts
59779-484-712024-08-14CVS Pharmacy, Inc. Pain Relief Drug Facts
59779-484-722024-08-14CVS Pharmacy, Inc. Pain Relief Drug Facts
59779-484-762024-08-14CVS Pharmacy, Inc. Pain Relief Drug Facts
59779-484-782024-08-14CVS Pharmacy, Inc. Pain Relief Drug Facts
59779-484-832024-08-14CVS Pharmacy, Inc. Pain Relief Drug Facts
59779-484-852024-08-14CVS Pharmacy, Inc. Pain Relief Drug Facts
59779-484-872024-08-14CVS Pharmacy, Inc. Pain Relief Drug Facts
59779-484-902024-08-14CVS Pharmacy, Inc. Pain Relief Drug Facts
59779-484-932024-08-14CVS Pharmacy, Inc. Pain Relief Drug Facts
59779-484-022024-01-30CVS Pharmacy, Inc. Pain Relief Drug Facts
59779-484-472024-01-30CVS Pharmacy, Inc. Pain Relief Drug Facts
59779-484-522024-01-30CVS Pharmacy, Inc. Pain Relief Drug Facts
59779-484-622024-01-30CVS Pharmacy, Inc. Pain Relief Drug Facts
59779-484-712024-01-30CVS Pharmacy, Inc. Pain Relief Drug Facts
59779-484-722024-01-30CVS Pharmacy, Inc. Pain Relief Drug Facts
59779-484-762024-01-30CVS Pharmacy, Inc. Pain Relief Drug Facts
59779-484-782024-01-30CVS Pharmacy, Inc. Pain Relief Drug Facts
59779-484-832024-01-30CVS Pharmacy, Inc. Pain Relief Drug Facts
59779-484-852024-01-30CVS Pharmacy, Inc. Pain Relief Drug Facts
59779-484-872024-01-30CVS Pharmacy, Inc. Pain Relief Drug Facts
59779-484-902024-01-30CVS Pharmacy, Inc. Pain Relief Drug Facts
59779-484-932024-01-30CVS Pharmacy, Inc. Pain Relief Drug Facts

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
59779-484-62EA - Each59779-4845f0b5831-8883-4870-b7b8-ee53633cdc7512018-10-11
59779-484-71EA - Each59779-484bc61e8b2-67b9-4fe5-ab6d-031df311732112018-10-11
59779-484-78EA - Each59779-484d5fd6556-0323-423d-bef9-d91e80cd3aba12018-10-11
59779-484-85EA - Each59779-48486e1f995-f3a7-4196-8c8b-54417bb7c30d12022-06-06
59779-484-93EA - Each59779-4847c4535b9-c496-4148-bddf-c0028c4622eb12018-12-13

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ACETAMINOPHENACTIVE INGREDIENT362O9ITL9DPAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN) TABLET [CVS PHARMACY]6
ACETAMINOPHENACTIVE MOIETY362O9ITL9DPAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN) TABLET [CVS PHARMACY]6
CARNAUBA WAXINACTIVE INGREDIENTR12CBM0EIZPAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN) TABLET [CVS PHARMACY]6
CROSCARMELLOSE SODIUMINACTIVE INGREDIENTM28OL1HH48PAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN) TABLET [CVS PHARMACY]6
HYPROMELLOSESINACTIVE INGREDIENT3NXW29V3WOPAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN) TABLET [CVS PHARMACY]6
POLYETHYLENE GLYCOLSINACTIVE INGREDIENT3WJQ0SDW1APAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN) TABLET [CVS PHARMACY]6
POVIDONESINACTIVE INGREDIENTFZ989GH94EPAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN) TABLET [CVS PHARMACY]6
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJPAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN) TABLET [CVS PHARMACY]6
STEARIC ACIDINACTIVE INGREDIENT4ELV7Z65APPAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN) TABLET [CVS PHARMACY]6

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
59779-484-9059779048490500 TABLET in 1 BOTTLE (59779-484-90) 500 tablet2015-09-150000-00-00NoNoCurrent