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
- 63629-7115_14931cd1-5c04-4801-aa6e-18138a21b28e
- Product NDC
- 63629-7115
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- Guaifenesin
- Labeler
- Bryant Ranch Prepack
- Marketing category
- NDA
- Marketing start / end (source format)
- 20120703
- Source listing expiry
- 20271231
Source-listed ingredients
- GUAIFENESIN — 600 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-7115-1) · 63629-7115-1
- 20 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-7115-2) · 63629-7115-2
- 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-7115-3) · 63629-7115-3
- 40 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-7115-4) · 63629-7115-4
- 14 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-7115-5) · 63629-7115-5
- 6 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-7115-6) · 63629-7115-6
- 10 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-7115-7) · 63629-7115-7
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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