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
- 71335-2642_bfd50410-1289-4b5d-86df-3b939d50bc27
- Product NDC
- 71335-2642
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- Guaifenesin
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190923
- Source listing expiry
- 20261231
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 (71335-2642-1) · 71335-2642-1
- 20 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2642-2) · 71335-2642-2
- 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2642-3) · 71335-2642-3
- 40 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2642-4) · 71335-2642-4
- 14 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2642-5) · 71335-2642-5
- 6 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2642-6) · 71335-2642-6
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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