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TUSSIN COUGH

NDC 76281-503 · AptaPharma Inc.

Generic nameDEXTROMETHORPHAN HYDROBROMIDE
Dosage formLIQUID
RouteORAL
Active ingredient(s)DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN
Strength10; 100 mg/5mL; mg/5mL
Pharmacologic classDecreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], Sigma-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

76281-503-24 — 118 mL in 1 BOTTLE (76281-503-24)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

76162-812 — Acetaminophen, Dextromethorphan hydrobromide, Doxylamine succinate, Phenylephrine hydrochloride, 76162-912 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 76162-913 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, Phenylephrine HCl, 76168-056 — Acetaminophen,Dextromethorphan,Doxylamine, 76281-304 — ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL, 76281-305 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, 76281-306 — ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL, 76281-307 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, 76281-501 — ACETAMINOPHEN, 76281-502 — ACETAMINOPHEN, 76281-504 — DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE, 76281-506 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 76281-507 — GUAIFENESIN, 76281-512 — DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, 76281-515 — ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCl, 76281-517 — Dextromethorphan HBr, GUaifenesin, Phenylephrine HCL, 76281-519 — ACETAMINOPHEN, DEXTROMETHORPHAN HBr, GUAIFENESIN, PHENYLEPHRINE HCL, 76281-601 — DEXTROMETHORPHAN HBr, GUAIFENESIN, 76281-603 — Acetaminophen,Dextromethrophan HBR,Doxylamine Succinate, 76281-604 — ACETAMINOPHEN, DEXTROMETHORPHAN HBr, PHENYLEPHRINE HCl, +2508 more

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