MUCUS RELIEF - DM

NDC 73581-405 · YYBA CORP

Generic nameGuaifenesin, Dextromethorphan HBr

Dosage formTABLET, EXTENDED RELEASE

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

73581-405-98 — 98 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (73581-405-98)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

73408-835 — Acetaminophen, Dextromethorphan HBr, Phenylephrine, Guaifenesin, ,, 73442-0012 — ginger, chlorheniramine maleate, dextromethorphan hydrobromide, 73442-0013 — lonicera flower, acetaminophen, dextromethorphan hydromide, 73442-0014 — citrus unshiu peel, saposhnikovia root, acetaminophen, dextromethorphan hydrobromide, 73564-801 — Guaifenesin, 73564-802 — Dextromethorphan, Guaifenesin, 73581-400 — Guaifenesin, 73581-401 — GUAIFENESIN, 73581-402 — GUAIFENESIN, 73581-403 — GUAIFENESIN, 73581-406 — Guaifenesin, Dextromethorphan HBr, 73598-1342 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride, 73629-005 — DEXTROMETHORPHAN HBR 15 MG, 75907-207 — Brompheniramine Maleate, Pseudoephedrine Hydrochloride, and Dextromethorphan Hydrobromide, 76095-012 — Guaifensin, Dextromethorphan, 76117-001 — CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE, 76162-000 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, 76162-004 — Guaifenesin 400mg, 76162-008 — Mucus Relief DM, 76162-026 — Nite Time Cold and Flu Relief, +2508 more

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