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DEXTROMETHORPHAN HBR 15 MG

NDC 73629-005 · AMZ789 LLC

Generic nameDEXTROMETHORPHAN HBR 15 MG
Dosage formCAPSULE, LIQUID FILLED
RouteORAL
Active ingredient(s)DEXTROMETHORPHAN HYDROBROMIDE
Strength15 mg/1
Pharmacologic classSigma-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

73629-005-10 — 100 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (73629-005-10)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

73097-011 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE, 73282-2523 — Dextromethorphan HBr, Guaifenesin, 73408-835 — Acetaminophen, Dextromethorphan HBr, Phenylephrine, Guaifenesin, ,, 73442-0012 — ginger, chlorheniramine maleate, dextromethorphan hydrobromide, 73442-0013 — lonicera flower, acetaminophen, dextromethorphan hydromide, 73442-0014 — citrus unshiu peel, saposhnikovia root, acetaminophen, dextromethorphan hydrobromide, 73564-802 — Dextromethorphan, Guaifenesin, 73581-405 — Guaifenesin, Dextromethorphan HBr, 73581-406 — Guaifenesin, Dextromethorphan HBr, 73598-1342 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride, 75907-207 — Brompheniramine Maleate, Pseudoephedrine Hydrochloride, and Dextromethorphan Hydrobromide, 76095-012 — Guaifensin, Dextromethorphan, 76117-001 — CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE, 76162-000 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, 76162-008 — Mucus Relief DM, 76162-026 — Nite Time Cold and Flu Relief, 76162-032 — GUAIFENESIN AND DEXTROMETHORPHAN HBR, 76162-040 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 76162-050 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 76162-057 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, +1967 more

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