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Bisolvine

NDC 53145-322 · MENPER DISTRIBUTORS INC.

Generic nameGuaifenesin, Dextromethorphan
Dosage formLIQUID
RouteORAL
Active ingredient(s)GUAIFENESIN, DEXTROMETHORPHAN HYDROBROMIDE
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

53145-322-04 — 1 BOTTLE in 1 CARTON (53145-322-04) / 120 mL in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

53041-617 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 53041-618 — Acteaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 53041-622 — Acteaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 53041-628 — Dextromethorphan HBr, Guaifenesin, 53113-514 — Dextromethorphan Hydrobromide, Guaifenesin, 53113-515 — Dextromethorphan Hydrobromide, Guaifenesin, 53145-026 — DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL, 53145-039 — Guaifenesin, Dextromethorphan HBR, 53145-059 — Dextromethorphan HBR, Guaifenesin, 53145-080 — Dextromethorphan Hydrobromide, Guaifenesin, 53145-323 — Guaifenesin, Dextromethorphan, 53145-333 — Dextromethorphan, Guiafenesin, Phenylephrine, 53145-402 — Dextromethorphan, Guaifenesin, 53145-691 — DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 53145-693 — DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 53145-695 — DEXTROMETHORPHAN HBr, GUAIFENESIN, PHENYLEPHRINE HCl, 53145-696 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin and Phenylephrine Hydrochloride, 53145-697 — DEXTROMETHORPHAN HBr, GUAIFENESIN, PHENYLEPHRINE HCL, 53163-101 — BROMPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE, 53163-104 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, +2508 more

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