Pain Reliever

NDC 68016-734 · CHAIN DRUG CONSORTIUM

Generic nameAcetaminophen

Dosage formTABLET, COATED

RouteORAL

Active ingredient(s)ACETAMINOPHEN

Strength500 mg/1

Marketing categoryOTC MONOGRAPH DRUG

Packages

68016-734-01 — 1 BOTTLE, PLASTIC in 1 CARTON (68016-734-01) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC

68016-734-22 — 225 TABLET, COATED in 1 BOTTLE, PLASTIC (68016-734-22)

68016-734-50 — 1 BOTTLE, PLASTIC in 1 CARTON (68016-734-50) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

67751-239 — Acetaminophen, Guaifenesin, and Phenylephrine Hydrochloride, 67751-240 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride, 67751-241 — acetaminophen and diphenhydramine hydrochloride, 67751-243 — Acetaminophen, Aspirin, and Caffeine, 68001-495 — Acetaminophen, 68016-154 — ACETAMINOPHEN, DIPHENHYDRAMINE HCL, PHENYLEPHRINE HCL, 68016-198 — Acetaminophen, 68016-303 — Acetaminophen, 68016-543 — Acetaminophen, 68016-654 — Acetaminophen Diphenhydramine HCl, 68016-797 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 68016-877 — Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, 68016-878 — Acetaminophen, Dextromethorphan HBr and Doxylamine Succinate, 68047-721 — butalbital and acetaminophen, 68047-752 — butalbital and acetaminophen, 68047-753 — butalbital and acetaminophen, 68071-2494 — Hydrocodone Bitartrate and Acetaminophen, 68071-2645 — Hydrocodone Bitartrate and Acetaminophen, 68071-3249 — Butalbital, Acetaminophen, and Caffeine, 68071-3437 — 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.