Acetaminophen

Product NDC
69848-008
11-digit product format
698480008
Labeler code
69848
Product ID
69848-008_468e7582-908f-6ec4-e063-6394a90a1653
Type
HUMAN OTC DRUG
Nonproprietary name
Acetaminophen
Dosage form
TABLET
Route
ORAL
Labeler
Granules USA, Inc
Application
M013
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2020-05-01
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

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69848-008-10Acetaminophen100 in 1 BOTTLETABLET1007

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69848-008ACETAMINOPHEN TABLET [GRANULES USA, INC]6Current NDC, Legacy NDC, 1 package rows20241218_a51395ea-e038-dc9c-e053-2a95a90a287d.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
198440acetaminophen 500 MG Oral TabletPSNa51395ea-e038-dc9c-e053-2a95a90a287d7
198440acetaminophen 500 MG Oral TabletSCDa51395ea-e038-dc9c-e053-2a95a90a287d7
198440APAP 500 MG Oral TabletSYa51395ea-e038-dc9c-e053-2a95a90a287d7

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69848-008-1069848000810100 TABLET in 1 BOTTLE (69848-008-10) 100 tablet2020-05-010000-00-00NoNoCurrent