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8 Hour Pain Relief

NDC 63868-679 · CHAIN DRUG MARKETING ASSOCIATION INC

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

Packages

63868-679-50 — 1 BOTTLE, PLASTIC in 1 CARTON (63868-679-50) / 50 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

63868-507 — Acetaminophen, 63868-567 — Acetaminophen, Chlorpheniramine maleate, Dextromethorphan HBr, 63868-578 — ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, and PHENYLEPHRINE HYDROCHLORIDE, 63868-582 — ACETAMINOPHEN and PHENYLEPHRINE HYDROCHLORIDE, 63868-587 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 63868-588 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 63868-589 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 63868-660 — Acetaminophen, 63868-677 — ACETAMINOPHEN, 63868-678 — ACETAMINOPHEN, 63868-722 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 63868-736 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 63868-737 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, 63868-746 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 63868-747 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 63868-809 — Acetaminophen, 63868-987 — Acetaminophen, 63941-095 — Acetaminophen and Diphenhydramine Hydrochloride, 63941-104 — Acetaminophen, 63941-159 — Acetaminophen, Aspirin and caffeine, +3476 more

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