ACETAMINOPHEN

Product NDC
11673-342
11-digit product format
116730342
Labeler code
11673
Product ID
11673-342_21331bbe-9573-2909-e063-6294a90abcee
Type
HUMAN OTC DRUG
Nonproprietary name
ACETAMINOPHEN
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
TARGET CORPORATION
Application
M013
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2019-06-01
Substance
ACETAMINOPHEN
Active strength
500 mg/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

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
ACETAMINOPHEN
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ACETAMINOPHEN500 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
362O9ITL9DInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
198440Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
80da2582-1a20-e111-e053-2991aa0acf32Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11673-342-01ACETAMINOPHEN100 in 1 BOTTLETABLET, FILM COATED1003
11673-342-26ACETAMINOPHEN225 in 1 BOTTLETABLET, FILM COATED2253
11673-342-42ACETAMINOPHEN24 in 1 BOTTLETABLET, FILM COATED243

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11673-342ACETAMINOPHEN TABLET, FILM COATED [TARGET CORPORATION]3Current NDC, Legacy NDC, 3 package rows20240927_80da2582-1a20-e111-e053-2991aa0acf32.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 59 of 79 · 1,579 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Pain Relief Regular StrengthACETAMINOPHENMARC GLASSMAN, INC.e21e821c-9694-5db0-e053-2995a90ad0342024-10-22WarningsExact identifier
application number: M013
Pain Relief Extra StrengthACETAMINOPHENMARC GLASSMAN, INC.e21e90e8-b9f1-1133-e053-2995a90a664b2024-10-22WarningsExact identifier
application number: M013
aspirinASPIRINPublix Super Markets Incc51dae48-aa49-4926-b04a-0da264e08dfa2024-10-22WarningsExact identifier
application number: M013
Acetaminophen Extra StrengthACETAMINOPHENKROGER COMPANYb96a2280-ec4f-7c61-e053-2995a90a18bb2024-10-22WarningsExact identifier
application number: M013
Pain Relief Extra StrengthACETAMINOPHENHEBf17a18b0-a7c2-4c64-868c-460cf34e1f7d2024-10-21WarningsExact identifier
application number: M013
Pain Relief Extra StrengthACETAMINOPHENHEB0863aeaa-15ec-4c67-ba79-4dad54555bd22024-10-21WarningsExact identifier
application number: M013
AcetaminophenACETAMINOPHENAmerican Health Packaging3c0175a0-175b-48b8-9192-3f869690c0f22024-10-21WarningsExact identifier
application number: M013
AcetaminophenACETAMINOPHENAmerican Health Packaging0d6553bd-3e18-4624-a83a-899bcafb32722024-10-21WarningsExact identifier
application number: M013
Childrens Acetaminophen Oral SuspensionACETAMINOPHENAmerican Health Packaging8231dd91-e9e6-4350-a485-fa95d65a6d252024-10-21WarningsExact identifier
application number: M013
Acetaminophen Extra StrengthACETAMINOPHENKROGER COMPANYcf63c372-acdd-6e6e-e053-2995a90a16622024-10-21WarningsExact identifier
application number: M013
good sense pain reliefACETAMINOPHENL. Perrigo Company8b56bfc0-2253-458d-99a6-0b0f9ae0ba502024-10-21WarningsExact identifier
application number: M013
AspirinASPIRINGOODSENSE662a2bc6-9507-465c-b467-7ae1b2e1dedc2024-10-18WarningsExact identifier
application number: M013
Pain Relief Extra StrengthACETAMINOPHENGoodSenseda4339c0-1822-41d8-8c20-214c379a5aa72024-10-18WarningsExact identifier
application number: M013
Pain Relief PM Extra StrengthACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDEGoodSense8972d95a-51da-40b5-8ef1-9dfed220d7eb2024-10-18WarningsExact identifier
application number: M013
Pain Relief Regular StrengthACETAMINOPHENAmeriSource Bergend571f520-a56e-4f7f-9214-d89197f742b62024-10-18WarningsExact identifier
application number: M013
LOW DOSE ASPIRINASPIRINBryant Ranch Prepack6b4b7f72-dac8-4b59-a58c-7c59d4b1ef322024-10-18WarningsExact identifier
application number: M013
dg health pain reliefACETAMINOPHENDolgencorp Inc2e1470f5-e88f-4d1d-a308-170f7080387e2024-10-17WarningsExact identifier
application number: M013
Pain ReliefACETAMINOPHENDISCOUNT DRUG MART146c735b-5081-4de4-9025-d939d560bbba2024-10-17WarningsExact identifier
application number: M013
Chewable AspirinASPIRINDISCOUNT DRUG MARTc8483d64-874c-3056-e053-2995a90ad8aa2024-10-17WarningsExact identifier
application number: M013
Adult Chewable AspirinASPIRINDISCOUNT DRUG MARTc8484998-e0e1-ffce-e053-2995a90aa7de2024-10-17WarningsExact identifier
application number: M013

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
198440acetaminophen 500 MG Oral TabletPSN80da2582-1a20-e111-e053-2991aa0acf323
198440acetaminophen 500 MG Oral TabletSCD80da2582-1a20-e111-e053-2991aa0acf323
198440APAP 500 MG Oral TabletSY80da2582-1a20-e111-e053-2991aa0acf323

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
11673-342-0111673034201100 TABLET, FILM COATED in 1 BOTTLE (11673-342-01) 2019-06-010000-00-00NoNoCurrent
11673-342-2611673034226225 TABLET, FILM COATED in 1 BOTTLE (11673-342-26) 2019-06-010000-00-00NoNoCurrent
11673-342-421167303424224 TABLET, FILM COATED in 1 BOTTLE (11673-342-42) 2019-06-010000-00-00NoNoCurrent