Acetaminophen Extra Strength

Product NDC
30142-033
11-digit product format
301420033
Labeler code
30142
Product ID
30142-033_abae08b0-d2ce-4263-9a67-5065a8a3059d
Type
HUMAN OTC DRUG
Nonproprietary name
Acetaminophen
Dosage form
TABLET
Route
ORAL
Labeler
KROGER COMPANY
Application
M013
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2022-02-02
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
30142-033-07Acetaminophen Extra Strength24 in 1 BOTTLETABLET245
30142-033-07Acetaminophen Extra Strength1 in 1 CARTONTABLET15

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
30142-033ACETAMINOPHEN EXTRA STRENGTH (ACETAMINOPHEN) TABLET [KROGER COMPANY]5Current NDC, Legacy NDC, 2 package rows20241024_cf63c372-acdd-6e6e-e053-2995a90a1662.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
198440acetaminophen 500 MG Oral TabletPSNcf63c372-acdd-6e6e-e053-2995a90a16625
198440acetaminophen 500 MG Oral TabletSCDcf63c372-acdd-6e6e-e053-2995a90a16625
198440APAP 500 MG Oral TabletSYcf63c372-acdd-6e6e-e053-2995a90a16625

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
30142-033-07301420033071 BOTTLE in 1 CARTON (30142-033-07) / 24 TABLET in 1 BOTTLE1 bottle2022-02-020000-00-00NoNoCurrent