Skip to main content

Acetaminophen

NDC 79481-0184 · MEIJER, INC.

Generic nameAcetaminophen
Dosage formTABLET
RouteORAL
Active ingredient(s)ACETAMINOPHEN
Strength650 mg/1
Marketing categoryANDA

Packages

79481-0184-1 — 100 TABLET in 1 BOTTLE (79481-0184-1)

79481-0184-8 — 24 TABLET in 1 BOTTLE (79481-0184-8)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

76420-876 — Hydrocodone Bitartrate and Acetaminophen, 76420-877 — Hydrocodone Bitartrate and Acetaminophen, 76420-914 — Acetaminophen tablet extended release, 76420-983 — Tramadol Hydrochloride and Acetaminophen, 79481-0045 — Acetaminophen, 79481-0110 — acetaminophen, dextromethorphan hydrobromide, 79481-0149 — Acetaminophen, Diphenhydramine hydrochloride, 79481-0152 — acetaminophen, ibuprofen, 79481-0174 — Acetaminophen, Diphenhydramine Hydrochloride, 79481-0183 — Acetaminophen, 79481-0203 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, 79481-0211 — acetaminophen, aspirin, caffeine, 79481-0302 — acetaminophen, 79481-0390 — Acetaminophen, Caffeine, Pyrilamine maleate, 79481-0503 — Acetaminophen, Ibuprofen, 79481-0780 — Acetaminophen, 79481-0807 — Acetaminophen, Dextromethorphan hydrobromide, Phenylephrine hydrochloride, 79481-0808 — Acetaminophen, Dextromethorphan hydrobromide, Doxylamine succinate, 79481-0827 — Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, 79481-0828 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, +3476 more

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