United States · FDA National Drug Code directory

Mucinex

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
67544-149_cc734890-e42c-454a-b771-3ecd169d161a
Product NDC
67544-149
Form
TABLET, EXTENDED RELEASE
Composition / generic term
Guaifenesin
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Marketing category
NDA
Marketing start / end (source format)
20120703
Source listing expiry
20261231

Source-listed ingredients

  • GUAIFENESIN — 600 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (67544-149-53) · 67544-149-53
  • 120 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (67544-149-70) · 67544-149-70
  • 180 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (67544-149-80) · 67544-149-80

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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