NDC 50580-608 – Tylenol PM Extra Strength

Acetaminophen 500 mg/1; Diphenhydramine Hydrochloride 25 mg/1 · Tablet, Film Coated · Oral

Human Otc Drug

Product NDC50580-608

Product details

Brand name
Tylenol PM Extra Strength
Generic name
Acetaminophen and diphenhydramine hydrochloride
Labeler
Kenvue Brands LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
OTC MONOGRAPH DRUG · M013
Marketed since
July 11, 2016
Listing expires
December 31, 2027
Pharmacologic class
Histamine-1 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Tylenol PM →

Package NDC codes (8)

Package NDCDescriptionSince
50580-608-011 BOTTLE in 1 CARTON (50580-608-01) / 24 TABLET, FILM COATED in 1 BOTTLEJul 11, 2016
50580-608-021 BOTTLE in 1 CARTON (50580-608-02) / 100 TABLET, FILM COATED in 1 BOTTLEJul 11, 2016
50580-608-031 BOTTLE in 1 CARTON (50580-608-03) / 150 TABLET, FILM COATED in 1 BOTTLEJul 11, 2016
50580-608-041 BOTTLE in 1 CARTON (50580-608-04) / 225 TABLET, FILM COATED in 1 BOTTLEJul 11, 2016
50580-608-052 TABLET, FILM COATED in 1 POUCH (50580-608-05)Jul 11, 2016
50580-608-0650 POUCH in 1 TRAY (50580-608-06) / 2 TABLET, FILM COATED in 1 POUCHJul 11, 2016
50580-608-072 POUCH in 1 CARTON (50580-608-07) / 2 TABLET, FILM COATED in 1 POUCHFeb 14, 2022
50580-608-081 BOTTLE in 1 CARTON (50580-608-08) / 50 TABLET, FILM COATED in 1 BOTTLEJun 1, 2022

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