pain reliever

Product NDC
0363-1502
11-digit product format
003631502
Labeler code
0363
Product ID
0363-1502_8446910d-7b7d-42d7-bdfd-8f2e7003c2fb
Type
HUMAN OTC DRUG
Nonproprietary name
acetaminophen
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Walgreen Company
Application
M013
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2022-09-02
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
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
0363-1502-78pain reliever100 in 1 BOTTLETABLET, FILM COATED1003
0363-1502-78pain reliever1 in 1 CARTONTABLET, FILM COATED13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0363-1502PAIN RELIEVER (ACETAMINOPHEN) TABLET, FILM COATED [WALGREEN COMPANY]3Current NDC, Legacy NDC, 2 package rows20240913_8255900a-2d58-4261-8df7-f28319883570.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
198440acetaminophen 500 MG Oral TabletPSN8255900a-2d58-4261-8df7-f283198835703
198440acetaminophen 500 MG Oral TabletSCD8255900a-2d58-4261-8df7-f283198835703
198440APAP 500 MG Oral TabletSY8255900a-2d58-4261-8df7-f283198835703

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0363-1502-78003631502781 BOTTLE in 1 CARTON (0363-1502-78) / 100 TABLET, FILM COATED in 1 BOTTLE1 bottle2022-09-020000-00-00NoNoCurrent