United States · FDA National Drug Code directory
Guaifenesin 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
- 43063-801_06c3176d-e6f9-4231-e063-6394a90a694b
- Product NDC
- 43063-801
- Form
- TABLET
- Composition / generic term
- GUAIFENESIN AND DEXTROMETHORPHAN HYDROBROMIDE
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20180402 / 20271130
Source-listed ingredients
- GUAIFENESIN — 400 mg/1
- DEXTROMETHORPHAN HYDROBROMIDE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE, PLASTIC (43063-801-30) · 43063-801-30
- 60 TABLET in 1 BOTTLE, PLASTIC (43063-801-60) · 43063-801-60
- 90 TABLET in 1 BOTTLE, PLASTIC (43063-801-90) · 43063-801-90
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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