Acetaminophen

Product NDC
72162-2164
11-digit product format
721622164
Labeler code
72162
Product ID
72162-2164_ce0027c4-cd60-4e48-96ce-9a12a2113f40
Type
HUMAN OTC DRUG
Nonproprietary name
Acetaminophen
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
M013
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2018-09-12
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
72162-2164-1Acetaminophen1 in 1 CARTONTABLET1101
72162-2164-1Acetaminophen100 in 1 BOTTLETABLET100101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72162-2164ACETAMINOPHEN TABLET [BRYANT RANCH PREPACK]101Current NDC, 2 package rows20240601_b5053cf5-209d-4106-afc2-cf9af85f4a69.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
198440acetaminophen 500 MG Oral TabletPSNb5053cf5-209d-4106-afc2-cf9af85f4a69101
198440acetaminophen 500 MG Oral TabletSCDb5053cf5-209d-4106-afc2-cf9af85f4a69101
198440APAP 500 MG Oral TabletSYb5053cf5-209d-4106-afc2-cf9af85f4a69101

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
72162-2164-1721622164011 BOTTLE in 1 CARTON (72162-2164-1) / 100 TABLET in 1 BOTTLE1 bottle2018-09-12NoNoHistorical