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Biocof

NDC 45737-249 · Advanced Generic Corporation

Generic nameDextromethorphan Hydrobromide, Guaifenesin, Phenylephrine HCL
Dosage formLIQUID
RouteORAL
Active ingredient(s)DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE
Strength20; 400; 10 mg/5mL; mg/5mL; mg/5mL
Pharmacologic classAdrenergic alpha1-Agonists [MoA], Decreased 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], alpha-1 Adrenergic Agonist [EPC]
Marketing categoryOTC MONOGRAPH DRUG

Packages

45737-249-16 — 473 mL in 1 BOTTLE (45737-249-16)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

43598-114 — Guaifenesin and Dextromethorphan HBR, 43598-115 — Guaifenesin and Dextromethorphan HBR, 43598-172 — Phenylephrine hydrochloride, 43598-199 — Phenylephrine hydrochloride, 43598-231 — Guaifenesin and Dextromethorphan HBR, 43598-232 — Guaifenesin and Dextromethorphan HBR, 43749-432 — PHENYLEPHRINE HYDROCHLORIDE, 45728-444 — Dextromethorphan HBr, 45728-445 — Nasal Decongestant, 45737-105 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 45737-250 — CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE, 45737-251 — Dextromethorphan Hydrobromide, Guaifenesin, 45802-188 — mineral oil, petrolatum, phenylephrine HCl, 45802-433 — dextromethorphan polistirex, 46122-136 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 46122-141 — dextromethorphan polistirex, 46122-198 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 46122-245 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 46122-410 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, and PHENYLEPHRINE HYDROCHLORIDE, 46122-412 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, +3082 more

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