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Acetaminophen, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride

NDC 68210-5053 · Prodose, Inc.

Generic nameAcetaminophen, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride
Dosage formCAPSULE, LIQUID FILLED
RouteORAL
Active ingredient(s)PHENYLEPHRINE HYDROCHLORIDE, ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE
Strength325; 10; 5 mg/1; mg/1; mg/1
Pharmacologic classAdrenergic alpha1-Agonists [MoA], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA], alpha-1 Adrenergic Agonist [EPC]
Marketing categoryOTC MONOGRAPH DRUG

Packages

68210-5053-1 — 2 POUCH in 1 CARTON (68210-5053-1) / 3000 CAPSULE, LIQUID FILLED in 1 POUCH

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68196-034 — Acetaminophen, 68196-177 — Acetaminophen, 68196-556 — acetaminophen, diphenhydramine HCl, 68196-606 — Acetaminophen, 68196-611 — acetaminophen, 68196-812 — dextromethorphan HBr, guaifenesin, 68196-919 — acetaminophen, 68196-935 — Acetaminophen, 68196-999 — Guaifenesin and Dextromethorphan HBR, 68210-4210 — Acetaminophen, Dextromethorphan hydrobromide, Doxylamine succinate, Phenylephrine hydrochloride, 68391-004 — Acetaminophen, 68391-288 — Acetaminophen, 68391-299 — Dextromethorphan HBr, Guaifenesin, 68391-411 — Acetaminophen, 68391-430 — Acetaminophen, Diphenhydramine, 68391-659 — Acetaminophen, 68391-711 — Dextromethorphan HBr, Guaifenesin, 68391-812 — dextromethorphan HBr, guaifenesin, 68391-863 — Acetaminophen, Diphenhydramine HCL, 68436-120 — Sorbutuss, +4867 more

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