United States · FDA National Drug Code directory
mucus relief
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
- 41250-684_097a3c6e-37e9-4380-ab8e-f458058014f4
- Product NDC
- 41250-684
- Form
- TABLET, MULTILAYER, EXTENDED RELEASE
- Composition / generic term
- Guaifenesin
- Labeler
- Meijer Distribution Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200807
- Source listing expiry
- 20261231
Source-listed ingredients
- GUAIFENESIN — 600 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 5 BLISTER PACK in 1 CARTON (41250-684-02) / 20 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BLISTER PACK · 41250-684-02
- 1 BOTTLE in 1 CARTON (41250-684-58) / 40 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BOTTLE · 41250-684-58
- 1 BOTTLE in 1 CARTON (41250-684-60) / 20 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BOTTLE · 41250-684-60
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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