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
- 51316-470_19d91bf6-33b2-4c00-9bc3-26c9f0c8e5df
- Product NDC
- 51316-470
- Form
- TABLET, MULTILAYER, EXTENDED RELEASE
- Composition / generic term
- guaifenesin
- Labeler
- CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250714
- Source listing expiry
- 20271231
Source-listed ingredients
- GUAIFENESIN — 600 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BLISTER PACK in 1 CARTON (51316-470-01) / 20 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BLISTER PACK · 51316-470-01
- 5 BLISTER PACK in 1 CARTON (51316-470-02) / 20 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BLISTER PACK · 51316-470-02
- 2 BLISTER PACK in 1 CARTON (51316-470-49) / 20 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BLISTER PACK · 51316-470-49
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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