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Mucus Relief DM Extended Release Caplets

NDC 63868-870 · QUALITY CHOICE (Chain Drug Marketing Association)

Generic nameGuaifenesin, Dextromethorphan HBr
Dosage formTABLET
RouteORAL
Active ingredient(s)DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN
Strength60; 1200 mg/1; mg/1
Pharmacologic classDecreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA]
Marketing categoryANDA

Packages

63868-870-14 — 14 BLISTER PACK in 1 CARTON (63868-870-14) / 1 TABLET in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

63868-736 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 63868-737 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, 63868-745 — dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 63868-746 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 63868-747 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 63868-753 — Dextromethorphan Hydrobromide / Guaifenesin, 63868-770 — Guaifenesin, 63868-771 — GUAIFENESIN and DEXTROMETHORPHAN HYDROBROMIDE, 63868-868 — Dextromethorphan HBr, Guaifenesin, 63868-869 — Dextromethorphan HBr, Guaifenesin, 63868-957 — Dextromethorphan HBr, 63868-998 — Guaifenesin, 63941-167 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 63941-173 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 63941-263 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 63941-274 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 63941-275 — Acetaminophen, Guaifenesin, Phenylephrine HCl, 63941-309 — Dextromethorphan HBr, 63941-343 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, 63941-344 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, +2508 more

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