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good sense cough dm

NDC 0113-0384 · L. Perrigo Company

Generic namedextromethorphan polistirex
Dosage formSUSPENSION
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

0113-0384-28 — 1 BOTTLE in 1 CARTON (0113-0384-28) / 148 mL in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0067-8127 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 0067-8132 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 0067-8136 — acetaminophen, dextromethorphan HBr, phenylephrine HCl, 0067-8145 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 0067-8204 — Acetaminophen, Dextromethorphan HBr, 0067-8205 — Acetaminophen, Chlorpheniramine maleate, Dextromethorphan HBr, 0067-8211 — ACETAMINOPHEN, DEXTROMETHORPHAN HBr, PHENYLEPHRINE HCl, 0113-0019 — Acetaminophen, dextromethorphan HBr, doxylamine succinate, phenylephrine HCl, 0113-0056 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 0113-0335 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 0113-0459 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 0113-0603 — acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl, 0113-0656 — acetaminophen, dextromethorphan Hbr, Phenylephrine HCl, 0113-0763 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, Phenylephrine HCl, 0113-0812 — dextromethorphan HBr, guaifenesin, 0113-0927 — Dextromethorphan HBr, Guaifenesin, 0113-0958 — dextromethorphan polistirex, 0113-0987 — Brompheniramine maleate, Dextromethorphan HBr, Phenylephrine HCl, 0113-0994 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 0113-1725 — dextromethorphan hydrobromide, guaifenesin, +1967 more

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