Guaifenesin and Dextromethorphan HBr

NDC 41415-998 · PUBLIX SUPER MARKETS, INC

Generic nameGuaifenesin and Dextromethorphan Hbr

Dosage formTABLET, EXTENDED RELEASE

RouteORAL

Active ingredient(s)GUAIFENESIN, DEXTROMETHORPHAN HYDROBROMIDE

Strength30; 600 mg/1; mg/1

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 categoryANDA

Packages

41415-998-20 — 1 BLISTER PACK in 1 CARTON (41415-998-20) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

41250-812 — dextromethorphan HBr, guaifenesin, 41250-869 — Acetaminophen, Dextromethorphan HBr, Triprolidine HCl, 41250-877 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, Phenylephrine HCl, 41250-899 — Dextromethorphan polistirex, 41250-958 — dextromethorphan polistirex, 41250-979 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 41250-981 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 41415-994 — Guaifenesin and Pseudoephedrine Hydrochloride, 41415-996 — Guaifenesin, 41415-997 — Guaifenesin, 41415-999 — Guaifenesin and Dextromethorphan HBr, 41520-032 — acetaminophen, dextromethorphan Hbr, Phenylephrine HCl, 41520-084 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 41520-138 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, and PHENYLEPHRINE HYDROCHLORIDE, 41520-384 — dextromethorphan polistirex, 41520-561 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, Phenylephrine HCl, 41520-603 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, and PHENYLEPHRINE HYDROCHLORIDE, 41520-712 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 41520-713 — acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl, 41520-731 — 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.

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