tussin dm nighttime max

NDC 42507-689 · HyVee Inc

Generic nameDextromethorphan Hydrobromide, Doxylamine Succinate

Dosage formSOLUTION

RouteORAL

Active ingredient(s)DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE

Strength30; 12.5 mg/20mL; mg/20mL

Pharmacologic classAntihistamine [EPC], Histamine Receptor Antagonists [MoA], 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

42507-689-26 — 1 BOTTLE in 1 CARTON (42507-689-26) / 118 mL in 1 BOTTLE (42507-689-00)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

42507-384 — dextromethorphan polistirex, 42507-401 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 42507-494 — dextromethorphan polistirex, 42507-511 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 42507-522 — acetaminophen, dextromethorphan Hbr, Phenylephrine HCl, 42507-532 — acetaminophen, dextromethorphan hydrobromide, 42507-581 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, 42507-603 — acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl, 42507-617 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 42507-630 — Dextromethorphan HBr, Guaifenesin, 42507-700 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 42507-727 — brompheniramine maleate, dextromethorphan hydrobromide, 42507-763 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, Phenylephrine HCl, 42507-811 — acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, 42507-812 — dextromethorphan HBr, guaifenesin, 42507-861 — acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, phenylephrine hydrochloride, 43063-801 — GUAIFENESIN AND DEXTROMETHORPHAN HYDROBROMIDE, 43598-114 — Guaifenesin and Dextromethorphan HBR, 43598-115 — Guaifenesin and Dextromethorphan HBR, 43598-231 — Guaifenesin and Dextromethorphan HBR, +2034 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