United States · FDA National Drug Code directory

Mucinex 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
63824-056_544ce67c-9f6a-7f3e-e063-6294a90ad619
Product NDC
63824-056
Form
TABLET, EXTENDED RELEASE
Composition / generic term
Guaifenesin and Dextromethorphan Hydrobromide
Labeler
Reckitt Benckiser LLC
Marketing category
NDA
Marketing start / end (source format)
20120626
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 (63824-056-32) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK · 63824-056-32
  • 2 BLISTER PACK in 1 CARTON (63824-056-34) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK · 63824-056-34
  • 1 BLISTER PACK in 1 CARTON (63824-056-36) / 6 TABLET, EXTENDED RELEASE in 1 BLISTER PACK · 63824-056-36
  • 3 BLISTER PACK in 1 CARTON (63824-056-69) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK · 63824-056-69
  • 2 TABLET, EXTENDED RELEASE in 1 POUCH (63824-056-72) · 63824-056-72
  • 24 POUCH in 1 CARTON (63824-056-74) / 2 TABLET, EXTENDED RELEASE in 1 POUCH (63824-056-73) · 63824-056-74
  • 2 BLISTER PACK in 1 CARTON (63824-056-80) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK · 63824-056-80

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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