United States · FDA National Drug Code directory

Duraflu

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: 50991-535_2683803e-5e2f-b2bc-e063-6394a90a4feb
Product NDC: 50991-535
Form: TABLET
Composition / generic term: ACETAMINOPHEN, DEXTROMETHORPHAN HBr, GUAIFENESIN, PSEUDOEPHEDRINE HCl
Labeler: Poly Pharmaceuticals, Inc.
Marketing category: OTC MONOGRAPH DRUG
Marketing start / end (source format): 20151001
Source listing expiry: 20261231

Source-listed ingredients

PSEUDOEPHEDRINE HYDROCHLORIDE — 60 mg/1
ACETAMINOPHEN — 325 mg/1
DEXTROMETHORPHAN HYDROBROMIDE — 20 mg/1
GUAIFENESIN — 200 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

100 TABLET in 1 BOTTLE (50991-535-01) · 50991-535-01
6 BLISTER PACK in 1 CARTON (50991-535-02) / 2 TABLET in 1 BLISTER PACK · 50991-535-02

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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