Acetaminophen Extra Strength

Product NDC
30142-165
11-digit product format
301420165
Labeler code
30142
Product ID
30142-165_0bd2025f-c8c1-690a-e063-6294a90a439c
Type
HUMAN OTC DRUG
Nonproprietary name
Acetaminophen
Dosage form
TABLET
Route
ORAL
Labeler
KROGER COMPANY
Application
M013
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2021-03-06
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 Extra Strength
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
30142-165-07Acetaminophen Extra Strength1 in 1 CARTONTABLET14
30142-165-07Acetaminophen Extra Strength24 in 1 BOTTLETABLET244

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
30142-165ACETAMINOPHEN EXTRA STRENGTH (ACETAMINOPHEN) TABLET [KROGER COMPANY]4Current NDC, Legacy NDC, 2 package rows20231207_b9b6f878-1ec8-3dc0-e053-2995a90a5414.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
198440acetaminophen 500 MG Oral TabletPSNb9b6f878-1ec8-3dc0-e053-2995a90a54144
198440acetaminophen 500 MG Oral TabletSCDb9b6f878-1ec8-3dc0-e053-2995a90a54144
198440APAP 500 MG Oral TabletSYb9b6f878-1ec8-3dc0-e053-2995a90a54144

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
30142-165-07301420165071 BOTTLE in 1 CARTON (30142-165-07) / 24 TABLET in 1 BOTTLE1 bottle2021-03-060000-00-00NoNoCurrent