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
- 51660-301_500a94a0-fecd-696a-e063-6394a90a931f
- Product NDC
- 51660-301
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- Guaifenesin and Dextromethorphan HBr
- Labeler
- OHM LABORATORIES INC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210701
- Source listing expiry
- 20271231
Source-listed ingredients
- GUAIFENESIN — 600 mg/1
- DEXTROMETHORPHAN HYDROBROMIDE — 30 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BLISTER PACK in 1 CARTON (51660-301-21) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK · 51660-301-21
- 2 BLISTER PACK in 1 CARTON (51660-301-41) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK · 51660-301-41
- 3 BLISTER PACK in 1 CARTON (51660-301-61) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK · 51660-301-61
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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