NDC 85237-2945 – Tylenol PM Extra Strength

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

Human Otc Drug

Product NDC85237-2945

Product details

Brand name
Tylenol PM Extra Strength
Generic name
Acetaminophen and diphenhydramine hydrochloride
Labeler
Select Consumer Group
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 (6)

Package NDCDescriptionSince
85237-2945-11 POUCH in 1 BLISTER PACK (85237-2945-1) / 2 TABLET, FILM COATED in 1 POUCH (85237-2945-0)Jun 1, 2022
85237-2945-22 POUCH in 1 BLISTER PACK (85237-2945-2) / 2 TABLET, FILM COATED in 1 POUCH (85237-2945-0)Jun 1, 2022
85237-2945-320 POUCH in 1 CONTAINER (85237-2945-3) / 2 TABLET, FILM COATED in 1 POUCH (85237-2945-0)Jun 1, 2022
85237-2945-425 POUCH in 1 CONTAINER (85237-2945-4) / 2 TABLET, FILM COATED in 1 POUCH (85237-2945-0)Jun 1, 2022
85237-2945-650 POUCH in 1 CONTAINER (85237-2945-6) / 2 TABLET, FILM COATED in 1 POUCH (85237-2945-0)Jun 1, 2022
85237-2945-73 POUCH in 1 BLISTER PACK (85237-2945-7) / 2 TABLET, FILM COATED in 1 POUCH (85237-2945-0)Jun 1, 2022

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