Acetaminophen

Product NDC
76168-120
11-digit product format
761680120
Labeler code
76168
Product ID
76168-120_6c311047-4be7-44ad-e053-2a91aa0ad047
Type
HUMAN OTC DRUG
Nonproprietary name
Acetaminophen
Dosage form
TABLET
Route
ORAL
Labeler
Velocity Pharma LLC
Application
part343
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2018-05-14
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
76168-120-10Acetaminophen60 in 1 BOTTLETABLET602
76168-120-10Acetaminophen1 in 1 CARTONTABLET12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76168-120ACETAMINOPHEN TABLET [VELOCITY PHARMA LLC]2Current NDC, Legacy NDC, 2 package rows20180515_bba2ddc5-19e0-4f11-8ff7-7dd7c2d53b50.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
198440acetaminophen 500 MG Oral TabletPSNbba2ddc5-19e0-4f11-8ff7-7dd7c2d53b502
198440acetaminophen 500 MG Oral TabletSCDbba2ddc5-19e0-4f11-8ff7-7dd7c2d53b502
198440APAP 500 MG Oral TabletSYbba2ddc5-19e0-4f11-8ff7-7dd7c2d53b502

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
76168-120-107616801201060 CARTON in 1 BOTTLE (76168-120-10) / 1 TABLET in 1 CARTON60 carton2018-05-140000-00-00NoNoCurrent