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Cough DM

NDC 59779-709 · CVS Pharmacy

Generic namedextromethorphan polistirex
Dosage formSUSPENSION, EXTENDED RELEASE
RouteORAL
Active ingredient(s)DEXTROMETHORPHAN HYDROBROMIDE
Strength30 mg/5mL
Pharmacologic classSigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA]
Marketing categoryANDA

Packages

59779-709-21 — 1 BOTTLE in 1 CARTON (59779-709-21) / 89 mL in 1 BOTTLE

59779-709-28 — 1 BOTTLE in 1 CARTON (59779-709-28) / 148 mL in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

59640-423 — acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, phenylephrine hydrochloride, 59726-733 — Guaifenesin, Dextromethorphan HBr, 59726-850 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 59726-899 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, 59779-335 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 59779-384 — dextromethorphan polistirex, 59779-459 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 59779-603 — acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl, 59779-648 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 59779-656 — acetaminophen, dextromethorphan hbr, phenylephrine hcl, 59779-763 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, Phenylephrine HCl, 59779-958 — dextromethorphan polistirex, 60000-057 — Guaifenesin and Dextromethorphan HBr, 60000-058 — Guaifenesin and Dextromethorphan HBr, 61787-070 — benzocaine and dextromethorphan HBr, 61787-515 — Dextromethorphan Hydrobromide and Guaifenesin, 62135-302 — Brompheniramine Maleate, Pseudoephedrine Hydrochloride, and Dextromethorphan Hydrobromide, 62559-758 — Promethazine Hydrochloride and Dextromethorphan Hydrobromide, 63102-101 — Dextromethorphan HBr,Guaifenesin,Pseudoephedrine HCl, 63102-102 — Dextromethorphan HBr,Guaifenesin,Pseudoephedrine 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.