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Guaifenesin and Dextromethorphan HBr

NDC 85766-046 · Sportpharm LLC

Generic nameGuaifenesin and Dextromethorphan HBr
Dosage formTABLET, EXTENDED RELEASE
RouteORAL
Active ingredient(s)GUAIFENESIN, DEXTROMETHORPHAN HYDROBROMIDE
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

85766-046-28 — 4 BLISTER PACK in 1 CARTON (85766-046-28) / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

84415-014 — Dextromethorphan HBr. and Guaifenesin, 84677-067 — Dextromethorphan Hydrobromide and Quinidine Sulphate, 85111-693 — Guaifenesin, 85111-802 — Dextromethorphan, Guaifenesin, 85237-1650 — Guaifenesin and Dextromethorphan Hydrobromide, 85237-1896 — ACETAMINOPHEN, DEXTROMETHORPHAN HBr, 85237-1955 — Acetaminophen, Guaifenesin, and Phenylephrine Hydrochloride, 85237-1956 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride, 85722-0001 — DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN, 85722-0002 — DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN, 85766-150 — Guaifenesin and Dextromethorphan HBr, 85766-162 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl ,, 85766-172 — dextromethorphan hydrobromide, guaifenesin, 85766-174 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, 85766-176 — Guaifenesin and Dextromethorphan Hydrobromide, 85766-177 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine succinate, 85766-179 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 85766-250 — Brompheniramine Maleate, Pseudoephedrine Hydrochloride, and Dextromethorphan Hydrobromide, 85786-301 — Guaifenesin, 85786-302 — Guaifenesin, +2508 more

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