Brompheniramine Maleate, Pseudoephedrine Hydrochloride and Dextromethorphan Hydrobromide

NDC 0574-1104 · Padagis US LLC

Generic nameBrompheniramine Maleate, Pseudoephedrine Hydrochloride and Dextromethorphan Hydrobromide

Dosage formSYRUP

RouteORAL

Active ingredient(s)BROMPHENIRAMINE MALEATE, PSEUDOEPHEDRINE HYDROCHLORIDE, DEXTROMETHORPHAN HYDROBROMIDE

Strength2; 10; 30 mg/5mL; mg/5mL; mg/5mL

Pharmacologic classAdrenergic alpha-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-Adrenergic Agonist [EPC]

Marketing categoryANDA

Packages

0574-1104-04 — 118 mL in 1 BOTTLE, PLASTIC (0574-1104-04)

0574-1104-16 — 473 mL in 1 BOTTLE, PLASTIC (0574-1104-16)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0536-1446 — dextromethorphan hydrobromide, guaifenesin, 0536-1447 — dextromethorphan hydrobromide, guaifenesin, 0536-1449 — guaifenesin and pseudoephedrine hydrochloride, 0536-1480 — Dextromethorphan Hydrobromide, 0536-1491 — fexofenadine hydrochloride, pseudoephedrine hydrochloride, 0536-3607 — Pseudoephedrine HCl, 0573-0180 — ibuprofen and pseudoephedrine hydrochloride, 0573-0184 — ibuprofen, pseudoephedrine hydrochloride, 0573-0188 — chlorpheniramine maleate, ibuprofen, pseudoephedrine HCl, 0573-2160 — ibuprofen and pseudoephedrine hydrochloride, 0713-0780 — Promethazine Hydrochloride and Dextromethorphan Hydrobromide, 0904-5053 — Pseudoephedrine HCl, 0904-5351 — Chlorpheniramine maleate, pseudoephedrine HCl, 0904-5786 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 0904-6312 — dextromethorphan polistirex, 0904-6337 — Pseudoephedrine HCl, 0904-6463 — Brompheniramine maleate, Dextromethorphan HBr, Phenylephrine HCl, 0904-6465 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 0904-6537 — Dextromethorphan HBr, Guaifenesin, Phenylephrine, 0904-6634 — Chlorpheniramine maleate, Dextromethorphan HBr, +2244 more

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

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels