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BupropiDex

NDC 71598-200 · DXM Pharmacuetical, Inc.

Generic nameDEXTROMETHORPHAN HYDROBROMIDE
Dosage formTABLET
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

71598-200-15 — 200 TABLET in 1 BOTTLE (71598-200-15)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71179-003 — Acetaminophen, Dextromethorphan hydrobromide and Doxylamine Succinate, 71179-011 — Guaifenesin and Dextromethorphan HBr, 71205-654 — Promethazine Hydrochloride and Dextromethorphan Hydrobromide Oral Solution, 71335-1928 — Guaifenesin and Dextromethorphan HBr, 71335-2216 — Dextromethorphan Hydrobromide / Guaifenesin, 71399-0025 — Dextromethorphan HBr, Guaifenesin, 71399-0026 — Dextromethorphan HBr, Guaifenesin, 71598-100 — Dextromethorphan Hbr, 71598-102 — Dextromethorphan HBr, 71598-152 — DEXTROMETHORPHAN HYDROBROMIDE, 71679-101 — acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride, 71679-102 — Acetaminophen, Doxylamine Succinate, Dextromethorphan HBr, 71800-057 — DEXTROMETHORPHAN HYDROBROMIDE,GUAIFENESIN, 71930-026 — Brompheniramine maleate, pseudoephedrine hydrochloride,, 71992-154 — ASPIRIN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE BITARTRATE, 72036-012 — Guaifenesin and Dextromethorphan HBr, 72036-138 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, and PHENYLEPHRINE HYDROCHLORIDE, 72036-155 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 72036-199 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 72036-274 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, +1967 more

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