Pain Reliever

Product NDC
71141-176
11-digit product format
711410176
Labeler code
71141
Product ID
71141-176_458b364a-a3ef-24ac-e063-6394a90ad1b8
Type
HUMAN OTC DRUG
Nonproprietary name
Acetaminophen
Dosage form
TABLET, COATED
Route
ORAL
Labeler
LIDL US LLC
Application
M013
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2022-11-23
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
Pain Reliever
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
71141-176-32Pain Reliever100 in 1 BOTTLE, PLASTICTABLET, COATED1005

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
198440acetaminophen 500 MG Oral TabletPSNec543339-20ab-2cba-e053-2995a90ac7405
198440acetaminophen 500 MG Oral TabletSCDec543339-20ab-2cba-e053-2995a90ac7405
198440APAP 500 MG Oral TabletSYec543339-20ab-2cba-e053-2995a90ac7405

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
71141-176-3271141017632100 TABLET, COATED in 1 BOTTLE, PLASTIC (71141-176-32) 2022-11-230000-00-00NoNoCurrent