United States · FDA National Drug Code directory
Duratuss AC
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
- 50991-540_3e5ed178-d5d8-b8d4-e063-6394a90a91db
- Product NDC
- 50991-540
- Form
- LIQUID
- Composition / generic term
- Codeine Phosphate, Dexbrompheniramine Maleate
- Labeler
- Poly Pharmaceuticals, Inc.
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20250908
- Source listing expiry
- 20261231
Source-listed ingredients
- CODEINE PHOSPHATE — 10 mg/5mL
- DEXBROMPHENIRAMINE MALEATE — 1 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 473 mL in 1 BOTTLE (50991-540-16) · 50991-540-16
- 20 mL in 1 BOTTLE (50991-540-20) · 50991-540-20
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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