BRONCOCHEM

NDC 65131-180 · LABORATORIO MAGNACHEM INTERNATIONAL SRL

Generic nameDEXTROMETHORPHAN HBr-GUAIFENESIN

Dosage formSYRUP

RouteORAL

Active ingredient(s)DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN

Strength10; 100 mg/15mL; mg/15mL

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 categoryOTC MONOGRAPH DRUG

Packages

65131-180-98 — 1 BOTTLE, PLASTIC in 1 BOX (65131-180-98) / 120 mL in 1 BOTTLE, PLASTIC

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

65131-011 — ACETAMINOPHEN-CHLORPHENIRAMINE MALEATE-DEXTROMETHORPHAN HBr-GUAIFENESIN-PHENYLEPHRINE HCl, 65131-035 — DEXTROMETHORPHAN HBR-PYRILAMINE MALEATE, 65131-054 — ACETAMINOPHEN-PHENYLEPHRINE HCl-GUAIFENESIN, 65131-091 — DEXTROMETHORPHAN HBr-GYAIFENESIN, 65131-100 — DEXTROMETHORPHAN HBr-GYAIFENESIN, 65131-101 — Acetaminophen-Dextromethorphan HBr-Phenylephrine HCl-Chlorpheniramine Maleate, 65131-109 — ACETAMINOPHEN-PHENYLEPHRINE HCl-GUAIFENESIN, 65131-110 — DEXTROMETHORPHAN HBR-PYRILAMINE MALEATE, 65131-111 — Acetaminophen-Dextromethorphan HBr-Phenylephrine HCl-Chlorpheniramine Maleate, 65131-116 — ACETAMINOPHEN-CHLORPHENIRAMINE MALEATE-DEXTROMETHORPHAN HBr-GUAIFENESIN-PHENYLEPHRINE HCl, 65131-418 — Chlorpheniramine maleate-Dextromethrophan HBr, 65162-036 — Guaifenesin, 65162-037 — Guaifenesin, 65162-038 — Guaifenesin and Dextromethorphan HBr, 65162-039 — Guaifenesin and Dextromethorphan HBr, 65162-680 — Promethazine Hydrochloride and Dextromethorphan Hydrobromide, 65162-700 — Dextromethorphan Polistirex, 65162-799 — Dextromethorphan Polistirex, 65852-002 — Chlorpheniramine Maleate, Dextromethorphan HBr, Phenylephrine HCL, 65852-003 — Dextromethorphan HBr, 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.