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NIGHTTIME SLEEP AID

NDC 59779-441 · CVS Pharmacy

Generic nameDoxylamine succinate
Dosage formTABLET
RouteORAL
Active ingredient(s)DOXYLAMINE SUCCINATE
Strength25 mg/1
Pharmacologic classAntihistamine [EPC], Histamine Receptor Antagonists [MoA]
Marketing categoryANDA

Packages

59779-441-01 — 1 BOTTLE in 1 CARTON (59779-441-01) / 96 TABLET in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

57243-501 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, 57243-502 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, 57243-603 — Acetaminophen, Dextromethorphan HBr and Doxylamine Succinate, 58593-003 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 58593-830 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, Phenylephrine HCl, 58602-769 — Acetaminophen, Dextromethorphan Hydrobromide and Doxylamine Succinate, 59450-047 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, 59640-423 — acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, phenylephrine hydrochloride, 59726-899 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, 59779-335 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 59779-459 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 59779-763 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, Phenylephrine HCl, 60665-003 — DOXYLAMINE SUCCINATE, 63629-2184 — Doxylamine Succinate and Pyridoxine Hydrochloride, Delayed release Tablets 10 mg/10 mg, 63868-140 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, 63868-234 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, 63868-292 — Dextromethorphan Hydrobromide, Doxylamine Succinate, 63868-418 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, 63868-737 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, 63941-343 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, +423 more

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