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Pain Relief

NDC 63868-082 · Chain Drug Marketing Association

FDA lists marketing as ended on 2026-08-31.
Generic nameAcetaminophen
Dosage formTABLET
RouteORAL
Active ingredient(s)ACETAMINOPHEN
Strength325 mg/1
Marketing categoryOTC MONOGRAPH DRUG

Packages

63868-082-10 — 1 BOTTLE, PLASTIC in 1 CARTON (63868-082-10) / 100 TABLET in 1 BOTTLE, PLASTIC

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

63824-950 — ACETAMINOPHEN, Diphenhydramine Hydrochloride, and Phenylephrine Hydrochloride, 63824-952 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride, 63824-954 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride, 63824-958 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride, 63824-959 — Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, and Triprolidine Hydrochloride, 63868-003 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 63868-020 — Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, 63868-032 — Acetaminophen, Caffeine, Pyrilamine maleate, 63868-071 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 63868-081 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 63868-084 — Acetaminophen, 63868-102 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 63868-103 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 63868-119 — Acetaminophen, Diphenhydramine HCl, 63868-140 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, 63868-174 — Acetaminophen, 63868-175 — Acetaminophen, 63868-186 — acetaminophen, 63868-210 — Acetaminophen, Diphenhydramine HCl, 63868-234 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, +3476 more