ACETAMINOPHEN 500 MG

NDC 72090-038 · Pioneer Life Sciences, LLC

Generic nameACETAMINOPHEN

Dosage formTABLET

RouteORAL

Active ingredient(s)ACETAMINOPHEN

Strength500 mg/1

Marketing categoryOTC MONOGRAPH DRUG

Packages

72090-038-01 — 500 TABLET in 1 BOTTLE (72090-038-01)

72090-038-02 — 300 TABLET in 1 PACKAGE (72090-038-02)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72036-305 — ACETAMINOPHEN, ASPIRIN and CAFFEINE, 72036-320 — ACETAMINOPHEN and PHENYLEPHRINE HYDROCHLORIDE, 72036-323 — ACETAMINOPHEN and PHENYLEPHRINE HYDROCHLORIDE, 72090-004 — ACETAMINOPHEN, CAFFEINE, 72090-005 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE, 72090-006 — ACETAMINOPHEN, DIPHENHYDRAMINE, 72090-007 — ACETAMINOPHEN, Aspirin, Caffeine, 72090-008 — ACETAMINOPHEN, 72090-026 — ACETAMINOPHEN, CAFFEINE, PYRILAMINE MALEATE, 72090-032 — ACETAMINOPHEN, DIPHENHYDRAMINE, 72090-062 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE, 72090-069 — Acetaminophen, 72162-1096 — butalbital, acetaminophen and caffeine, 72162-1232 — butalbital, acetaminophen and caffeine, 72162-1279 — Hydrocodone Bitartrate and Acetaminophen, 72162-1280 — Hydrocodone Bitartrate and Acetaminophen, 72162-1281 — Hydrocodone Bitartrate and Acetaminophen, 72162-1287 — Hydrocodone Bitartrate and Acetaminophen, 72162-1288 — Hydrocodone Bitartrate and Acetaminophen, 72162-1289 — Hydrocodone Bitartrate and Acetaminophen, +3478 more

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