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DG Health Cough DM

NDC 55910-384 · Dolgencorp Inc

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

55910-384-21 — 1 BOTTLE in 1 CARTON (55910-384-21) / 89 mL in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

55910-146 — Dextromethorphan HBr, Guaifenesin, 55910-149 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, 55910-272 — Dextromethorphan Hydrobromide / Guaifenesin, 55910-297 — Acetaminophen, Chlorpheniramine maleate, Dextromethorphan hydrobromide, 55910-300 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 55910-309 — Dextromethorphan HBr, 55910-335 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 55910-336 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 55910-366 — Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, 55910-378 — Dextromethorphan HBr, Phenylephrine HCl, 55910-398 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, 55910-432 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 55910-443 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, 55910-459 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 55910-505 — Dextromethorphan HBr, Guaifenesin, 55910-509 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 55910-515 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, 55910-533 — Dextromethorphan HBr, Guaifenesin, 55910-537 — dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 55910-575 — dextromethorphan HBr, 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.

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels