NDC 50580-378 – Tylenol Extra Strength

Acetaminophen 500 mg/1 · Tablet, Film Coated · Oral

Human Otc Drug 1 recall

Product NDC50580-378

Product details

Brand name
Tylenol Extra Strength
Generic name
Acetaminophen
Labeler
Kenvue Brands LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
OTC MONOGRAPH DRUG · M013
Marketed since
November 1, 2014
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for TYLENOL Extra Strength →

Package NDC codes (9)

Package NDCDescriptionSince
50580-378-011 BOTTLE, PLASTIC in 1 CARTON (50580-378-01) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTICNov 1, 2014
50580-378-021 BOTTLE, PLASTIC in 1 CARTON (50580-378-02) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTICNov 1, 2014
50580-378-03225 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50580-378-03)Apr 6, 2015
50580-378-041 BOTTLE, PLASTIC in 1 CARTON (50580-378-04) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTICMar 1, 2021
50580-378-051 BOTTLE, PLASTIC in 1 CARTON (50580-378-05) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTICMar 1, 2021
50580-378-061 BOTTLE, PLASTIC in 1 CARTON (50580-378-06) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTICMar 1, 2021
50580-378-071 BOTTLE, PLASTIC in 1 CARTON (50580-378-07) / 225 TABLET, FILM COATED in 1 BOTTLE, PLASTICMar 1, 2021
50580-378-08325 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50580-378-08)Mar 1, 2021
50580-378-37320 TABLET, FILM COATED in 1 BOTTLE (50580-378-37)Mar 31, 2026

Recalls mentioning this NDC

Other TYLENOL Extra Strength products