Tylenol Extra Strength

Product NDC
50580-472
11-digit product format
505800472
Labeler code
50580
Product ID
50580-472_21c39261-4b98-bc43-e063-6394a90a4eb8
Type
HUMAN OTC DRUG
Nonproprietary name
Acetaminophen
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Kenvue Brands LLC
Application
M013
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2024-03-18
Substance
ACETAMINOPHEN
Active strength
500 mg/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
362O9ITL9DACETAMINOPHEN103-90-2ACETAMINOPHEN

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
50580-472-01505800472011 BOTTLE in 1 CARTON (50580-472-01) / 24 TABLET, FILM COATED in 1 BOTTLE1 bottle2024-03-18NoNoHistorical
50580-472-02505800472021 BOTTLE in 1 CARTON (50580-472-02) / 50 TABLET, FILM COATED in 1 BOTTLE1 bottle2024-03-18NoNoHistorical
50580-472-03505800472031 BOTTLE in 1 CARTON (50580-472-03) / 100 TABLET, FILM COATED in 1 BOTTLE1 bottle2024-03-18NoNoHistorical
50580-472-04505800472041 BOTTLE in 1 CARTON (50580-472-04) / 200 TABLET, FILM COATED in 1 BOTTLE1 bottle2024-03-18NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Tylenol ® Extra StrengthKenvue Brands LLC2024-11-07HUMAN OTC DRUG LABEL2