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WALGREENS

NDC 0363-8100 · WALGREENS CO.

Generic nameacetaminophen, dextromethorphan hydrobromide
Dosage formLIQUID
RouteORAL
Active ingredient(s)ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE
Strength650; 20 mg/30mL; mg/30mL
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

0363-8100-12 — 355 mL in 1 BOTTLE (0363-8100-12)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0363-7560 — Nighttime Cough, 0363-7754 — Dextromethorphan HBr, Guaifenesin, 0363-7760 — dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride, 0363-7920 — Acetaminophen, Chlorpheniramine Maleate, and Dextromethorphan Hydrobromide, 0363-8004 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 0363-8005 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 0363-8031 — Dextromethorphan HBr, Guaifenesin, 0363-8063 — Acetaminophen, Dextromethorphan HBr, Triprolidine HCl, 0363-8078 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, Triprolidine HCl, 0363-8079 — Acetaminophen, 0363-8990 — DEXTROMETHORPHAN HBr, 0363-8992 — ACETAMINOPHEN, ASPIRIN, CAFFEINE, 0363-8996 — ACETAMINOPHEN, GUAIFENESIN, DEXTROMETHORPHAN HYDROBROMIDE, and PHENYLEPHRINE HYDROCHLORIDE, 0363-8997 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, and PHENYLEPHRINE HYDROCHLORIDE, 0363-8998 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, and PHENYLEPHRINE HYDROCHLORIDE, 0363-8999 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, and DOXYLAMINE SUCCINATE, 0363-9013 — GUAIFENESIN and DEXTROMETHORPHAN HYDROBROMIDE, 0363-9016 — ACETAMINOPHEN, GUAIFENESIN, DEXTROMETHORPHAN HYDROBROMIDE, and PHENYLEPHRINE HYDROCHLORIDE, 0363-9017 — ACETAMINOPHEN, GUAIFENESIN, DEXTROMETHORPHAN HYDROBROMIDE, and PHENYLEPHRINE HYDROCHLORIDE, 0363-9019 — Acetaminophen, Dextromethorphan hydrobromide, and Phenylephrine hydrochloride, +4418 more

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