United States · FDA National Drug Code directory
equate mucus-er
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
- 79903-292_8800c85b-3527-4480-8101-cde32bd6ccd2
- Product NDC
- 79903-292
- Form
- TABLET, MULTILAYER, EXTENDED RELEASE
- Composition / generic term
- guaifenesin
- Labeler
- WALMART INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250218
- Source listing expiry
- 20271231
Source-listed ingredients
- GUAIFENESIN — 600 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (79903-292-06) / 20 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BOTTLE · 79903-292-06
- 1 BOTTLE in 1 CARTON (79903-292-12) / 40 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BOTTLE · 79903-292-12
- 1 BLISTER PACK in 1 CARTON (79903-292-20) / 20 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BLISTER PACK · 79903-292-20
- 2 BLISTER PACK in 1 CARTON (79903-292-40) / 20 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BLISTER PACK · 79903-292-40
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →