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Sanatos

NDC 55758-416 · Pharmadel LLC

Generic nameAcetaminophen, Dextromethorphan HBr, Doxylamine Succinate
Dosage formLIQUID
RouteORAL
Active ingredient(s)ACETAMINOPHEN, DOXYLAMINE SUCCINATE, DEXTROMETHORPHAN HYDROBROMIDE
Strength650; 30; 12.5 mg/30mL; mg/30mL; mg/30mL
Pharmacologic classAntihistamine [EPC], Histamine Receptor Antagonists [MoA], 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

55758-416-06 — 177 mL in 1 BOTTLE, PLASTIC (55758-416-06)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

55758-322 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 55758-323 — DEXTROMETHORPHAN HBR, 55758-326 — Acetaminophen, Caffeine, Pyrilamine Maleate, 55758-361 — Acetaminophen, dextromethorphan HBr, guaifenesin, phenylephrine HCI, 55758-381 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCL, 55758-382 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, Phenylephrine HCL, 55758-384 — Acetaminophen, Dextromethorphan hydrobromide, and Phenylephrine hydrochloride, 55758-385 — Acetaminophen, Diphenhydramine hydrochloride, and Phenylephrine hydrochloride, 55758-407 — Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan HBr, Phenylephrine HCl,, 55758-415 — Acetaminophen, Dextromethorphan HBr, 55758-432 — Acetaminophen, Chlorpheniramine maleate, Dextromethorphan HBr, 55758-435 — Acetaminophen, Caffeine, 55758-439 — ACETAMINOPHEN, 55758-443 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCi, 55758-500 — Acetaminophen, Chlorpheniramine maleate, Phenylephrine HCl, 55758-501 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 55758-502 — Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan HBr, Phenylephrine HCl, 55758-503 — ACETAMINOPHEN, 55758-507 — Dextromethorphan HBr, Guaifenesin, 55758-508 — Acetaminophen, Dextromethorphan, Phenylephrine, +4482 more

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