Acetaminophen

Product NDC
84269-2522
11-digit product format
842692522
Labeler code
84269
Product ID
84269-2522_df0b3333-813c-483c-9e44-7a1b3b70d7b1
Type
HUMAN OTC DRUG
Nonproprietary name
Acetaminophen
Dosage form
TABLET
Route
ORAL
Labeler
Wildman Business Group
Application
M013
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2024-05-20
Substance
ACETAMINOPHEN
Active strength
500 mg/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

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 Identifiers#

Field, Values table
FieldValues
Unii362O9ITL9D
Rxcui198440

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84269-2522-1Acetaminophen2 in 1 PACKETTABLET21
84269-2522-1Acetaminophen50 in 1 BOXTABLET501
84269-2522-2Acetaminophen125 in 1 BOXTABLET1251
84269-2522-2Acetaminophen2 in 1 PACKETTABLET21

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84269-2522ACETAMINOPHEN TABLET [WILDMAN BUSINESS GROUP]1Current NDC, 4 package rows20240523_943c8f49-e65e-40bc-b364-3274df4d21a2.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
198440acetaminophen 500 MG Oral TabletPSN943c8f49-e65e-40bc-b364-3274df4d21a21
198440acetaminophen 500 MG Oral TabletSCD943c8f49-e65e-40bc-b364-3274df4d21a21
198440APAP 500 MG Oral TabletSY943c8f49-e65e-40bc-b364-3274df4d21a21

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
84269-2522-18426925220150 PACKET in 1 BOX (84269-2522-1) / 2 TABLET in 1 PACKET50 packet2024-05-20NoNoHistorical
84269-2522-284269252202125 PACKET in 1 BOX (84269-2522-2) / 2 TABLET in 1 PACKET125 packet2024-05-20NoNoHistorical