United States · FDA National Drug Code directory

DURATUSS DM

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference: 50991-142_413a3951-d703-f14b-e063-6394a90a06dc
Product NDC: 50991-142
Form: LIQUID
Composition / generic term: Dexbrompheniramine Maleate, Dextromethorphan Hydrobromide and Pseudoephedrine Hydrochloride
Labeler: Poly Pharmaceuticals, Inc.
Marketing category: OTC MONOGRAPH DRUG
Marketing start / end (source format): 20251015
Source listing expiry: 20261231

Source-listed ingredients

DEXBROMPHENIRAMINE MALEATE — 1 mg/5mL
DEXTROMETHORPHAN HYDROBROMIDE — 10 mg/5mL
PSEUDOEPHEDRINE HYDROCHLORIDE — 30 mg/5mL

These values do not establish equivalence or a dose recommendation.

Packages

473 mL in 1 BOTTLE (50991-142-16) · 50991-142-16
20 mL in 1 BOTTLE (50991-142-20) · 50991-142-20

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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