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
- 58602-825_f2b5fe0d-e42b-453f-920e-f7db45219f21
- Product NDC
- 58602-825
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- Guaifenesin and Dextromethorphan HBr
- Labeler
- Aurohealth LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170317
- Source listing expiry
- 20261231
Source-listed ingredients
- GUAIFENESIN — 1200 mg/1
- DEXTROMETHORPHAN HYDROBROMIDE — 60 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 6 BLISTER PACK in 1 CARTON (58602-825-06) / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK · 58602-825-06
- 2 BLISTER PACK in 1 CARTON (58602-825-65) / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK · 58602-825-65
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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