United States · FDA National Drug Code directory
Guaifenesin and Dextromethorphan HBr
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
- 71179-011_161614f9-ae67-454a-bf7f-dfc6ec40f8de
- Product NDC
- 71179-011
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- Guaifenesin and Dextromethorphan HBr
- Labeler
- VESPYR BRANDS LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220714
- Source listing expiry
- 20271231
Source-listed ingredients
- GUAIFENESIN — 1200 mg/1
- DEXTROMETHORPHAN HYDROBROMIDE — 60 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 3 BLISTER PACK in 1 CARTON (71179-011-21) / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK · 71179-011-21
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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