Premier Value

NDC 68016-744 · PHARMACY VALUE ALLIANCE LLC

Generic nameDextromethorphan HBr, Guaifenesin

Dosage formSOLUTION

RouteORAL

Active ingredient(s)DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN

Strength20; 200 mg/20mL; mg/20mL

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

68016-744-04 — 1 BOTTLE in 1 CARTON (68016-744-04) / 118 mL in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

67544-149 — Guaifenesin, 67751-171 — DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, 67751-217 — chlorpheniramine maleate, acetaminophen, phenylephrine hydrochloride, dextromethorphan hydrobromide, 67751-239 — Acetaminophen, Guaifenesin, and Phenylephrine Hydrochloride, 67751-240 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride, 67877-558 — Brompheniramine, Pseudoephedrine, Dextromethorphan, 68001-561 — Guaifenesin, 68016-674 — Guaifenesin, Dextromethorphan HBr, 68016-740 — Dextromethorphan HBr, Guaifenesin, 68016-742 — Dextromethorphan HBr, 68016-797 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 68016-877 — Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, 68016-878 — Acetaminophen, Dextromethorphan HBr and Doxylamine Succinate, 68047-129 — Brompheniramine Maleate, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride, 68047-143 — Brompheniramine Maleate, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride, 68047-186 — Chlorpheniramine Maleate, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride, 68071-3551 — Promethazine Hydrochloride and Dextromethorphan Hydrobromide Oral Solution, 68071-3938 — Dextromethorphan HBr, Guaifenesin, 68071-5173 — Codeine Phosphate and Guaifenesin, 68084-572 — Guaifenesin, +2508 more

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