Acetaminophen

Product NDC
72789-267
11-digit product format
727890267
Labeler code
72789
Product ID
72789-267_2e5d566b-3e9d-35bd-e063-6294a90a0513
Type
HUMAN OTC DRUG
Nonproprietary name
Acetaminophen
Dosage form
TABLET
Route
ORAL
Labeler
PD-Rx Pharmaceuticals, Inc.
Application
M013
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2021-03-11
Substance
ACETAMINOPHEN
Active strength
325 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
ACETAMINOPHEN325 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
313782Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
da7d95af-6583-429d-8d04-e0424f32e9adAvailable on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72789-267-20Acetaminophen20 in 1 BOTTLE, PLASTICTABLET207
72789-267-30Acetaminophen30 in 1 BOTTLE, PLASTICTABLET307

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
72789-267-20EA - Each72789-26740155d8e-5afc-43c1-8062-827a1bca434512022-10-06
72789-267-30EA - Each72789-2678a6851d3-9603-4262-bab0-f750b098c73d12023-06-06

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72789-267ACETAMINOPHEN TABLET [PD-RX PHARMACEUTICALS, INC.]7Current NDC, Legacy NDC, 2 package rows20250221_da7d95af-6583-429d-8d04-e0424f32e9ad.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
313782acetaminophen 325 MG Oral TabletPSNda7d95af-6583-429d-8d04-e0424f32e9ad7
313782acetaminophen 325 MG Oral TabletSCDda7d95af-6583-429d-8d04-e0424f32e9ad7
313782APAP 325 MG Oral TabletSYda7d95af-6583-429d-8d04-e0424f32e9ad7

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
72789-267-207278902672020 TABLET in 1 BOTTLE, PLASTIC (72789-267-20) 20 tablet2022-08-010000-00-00NoNoCurrent
72789-267-307278902673030 TABLET in 1 BOTTLE, PLASTIC (72789-267-30) 30 tablet2023-04-05NoNoCurrent