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CVS Health COUGH SUPPRESSANT SOFTGEL

NDC 51316-877 · CVS Pharmacy, Inc.

Generic nameDextromethorphan hydrobromide
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

51316-877-23 — 1 BOTTLE, PLASTIC in 1 CARTON (51316-877-23) / 20 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

51316-752 — Chlorpheniramine maleate and Dextromethorphan Hydrobromide, 51316-775 — Dextromethorphan HBr, Guaifenesin, 51316-778 — Dextromethorphan Hydrobromide, 51316-791 — Dextromethorphan Hydrobromide, Doxylamine Succinate, 51316-803 — Acetaminophen, Dextromethorphan HBr, 51316-808 — Dextromethorphan HBr, Guaifenesin, 51316-815 — Dextromethorphan HBr, guaifenesin, Phenylephrine HCl, 51316-826 — Dextromethorphan Hydrobromide, Guaifenesin, 51316-830 — Dextromethorphan hydrobromide, Guaifenesin, 51316-858 — dextromethorphan hydrobromide, guaifenesin, 51316-884 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine succinate, 51316-896 — Acetaminophen Dextromethorphan HBr Phenylephrine HCl, 51316-897 — Acetaminophen, Dextromethorphan HBr, 51316-921 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine succinate, 51316-943 — dextromethorphan polistirex, 51316-945 — Acetaminophen, Chlorpheniramine Maleate and Dextromethophan HBr, 51316-963 — Acetaminophen, Dextromethorphan HBr, Triprolidine HCl, 51467-007 — ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE, 51467-012 — Acetaminophen, Chlorpheniramine maleate, Dextromethorphan Hydrobromide, Phenylephrine hydrochloride, 51660-110 — Guaifenesin and Dextromethorphan HBr, +1967 more

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