ED-A-HIST DM

NDC 0485-0240 · EDWARDS PHARMACEUTICALS, INC.

Generic nameCHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, and PHENYLEPHRINE HYDROCHLORIDE

Dosage formTABLET, COATED

RouteORAL

Active ingredient(s)CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE

Strength4; 10; 10 mg/1; mg/1; mg/1

Pharmacologic classAdrenergic alpha1-Agonists [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], 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 categoryUNAPPROVED DRUG OTHER

Packages

0485-0240-01 — 100 TABLET, COATED in 1 BOTTLE, PLASTIC (0485-0240-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0363-9976 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, 0395-9126 — Dextromethorphan HBr, 0404-9931 — Phenylephrine Hydrochloride, 0485-0080 — DEXCHLORPHENIRAMINE MALEATE and PHENYLEPHRINE HYDROCHLORIDE, 0485-0098 — CHLORPHENIRAMINE MALEATE, 0485-0155 — Chlorpheniramine/Phenylephrine, 0485-0171 — DEXTROMETHORPHAN HYDROBROMIDE, CHLORPHENIRAMINE MALEATE, and PHENYLEPHRINE HYDROCHLORIDE, 0485-0202 — BROMPHENIRAMINE MALEATE and Phenylephrine HCL, 0485-0204 — Brompheniramine Maleate, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, 0485-0208 — GUAIFENESIN and PHENYLEPHRINE, 0485-0254 — CHLORPHENIRAMINE MALEATE and PHENYLEPHRINE HYDROCHLORIDE, 0496-0978 — lidocaine and mineral oil and phenylephrine HCl and white petrolatum, 0536-1006 — Chlorpheniramine Maleate, 0536-1161 — Guaifenesin, Dextromethorphan HBr, 0536-1186 — cocoa butter, phenylephrine HCl, 0536-1213 — Guaifenesin, Dextromethorphan HBr, 0536-1288 — Mineral Oil, Petrolatum, Phenylephrine HCI, 0536-1289 — Acetaminophen, Phenylephrine HCl, 0536-1309 — Guaifenesin/phenylephrine, 0536-1312 — Dextromethorphan Hydrobromide / Guaifenesin, +2759 more

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