TYLENOL PM EXTRA STRENGTH

NDC 70264-028 · R J General Corporation

Generic nameACETAMINOPHEN

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE

Strength500; 25 mg/1; mg/1

Pharmacologic classHistamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]

Marketing categoryOTC MONOGRAPH DRUG

Packages

70264-028-01 — 50 POUCH in 1 BOX (70264-028-01) / 2 TABLET, FILM COATED in 1 POUCH

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70038-131 — Acetaminophen, 70040-0145 — Benzhydrocodone and Acetaminophen, 70040-0167 — Benzhydrocodone and Acetaminophen, 70040-0189 — Benzhydrocodone and Acetaminophen, 70264-012 — acetaminophen, caffeine, and pyrilamine maleate, 70264-016 — chlorpheniramine maleate, acetaminophen, phenylephrine hydrochloride, dextromethorphan hydrobromide, 70264-024 — DIPHENHYDRAMINE HYDROCHLORIDE, 70264-025 — ACETAMINPHEN, 70264-026 — ACETAMINOPHEN, 70264-027 — ACETAMINOPHEN, 70264-040 — Acetaminophen 250 mg and Ibuprofen 125 mg, 70264-045 — Acetaminophen, Aspirin (NSAID), Caffeine, 70264-047 — ACETAMINOPHEN, DEXTROMETHORPHAN HBr, 70518-1082 — diphenhydramine hydrochloride, 70518-1134 — Butalbital, Acetaminophen, and Caffeine, 70518-2628 — acetaminophen and codeine phosphate, 70518-2764 — acetaminophen and codeine phosphate, 70518-3705 — acetaminophen and codeine phosphate, 70518-4104 — Acetaminophen and Codeine Phosphate, 70518-4184 — Acetaminophen, +4330 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.