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Triponel

NDC 54859-508 · LLORENS PHARMACEUTICALS INTERNATIONAL DIVISION

Generic nameDextromethorphan HBr, Phenylephrine HCl, Triprolidine HCl
Dosage formLIQUID
RouteORAL
Active ingredient(s)DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE, TRIPROLIDINE HYDROCHLORIDE
Strength15; 5; 1.25 mg/5mL; mg/5mL; mg/5mL
Pharmacologic classAdrenergic alpha1-Agonists [MoA], 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

54859-508-16 — 474 mL in 1 BOTTLE (54859-508-16)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

53943-517 — DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE, 53943-518 — DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, 53943-603 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, 53943-689 — Chlorpheniramine maleate, Dextromethorphan HBr, 54257-277 — DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, 54738-985 — Guaifenesin and Dextromethorphan HBr, 54859-011 — Dextromethorphan HBr, Guaifenesin, 54859-502 — Dextromethorphan, Guiafenesin, Pseudoephedrine HCl, 54859-505 — Dextromethorphan, Guaifenesin, 54859-506 — Dextromethorphan HBr, Guaifenesin, 54859-509 — Dextromethorphan HBr, Guaifenesin, 54859-514 — Dextromethorphan HBr, Pseufoephedrine HCl, Triprolidine HCl, 54859-517 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 54859-544 — Dextromethorphan, Guiafenesin, Pseudoephedrine HCl, 54859-603 — Dextromethorphan, Guiafenesin, Pseudoephedrine HCl, 54859-604 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 54859-605 — Guaifenesin, Phenylephrine HCl, 54859-606 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 54859-833 — Dextromethorphan HBr, Guaifenesin, 55150-300 — Phenylephrine Hydrochloride, +2678 more

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