United States · FDA National Drug Code directory
GUAIFENESIN
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
- 0121-1744_25a970c7-0016-4f22-9e94-1e20e1319e3e
- Product NDC
- 0121-1744
- Form
- SOLUTION
- Composition / generic term
- GUAIFENESIN
- Labeler
- PAI Holdings, LLC dba PAI Pharma
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20020901
- Source listing expiry
- 20261231
Source-listed ingredients
- GUAIFENESIN — 100 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 TRAY in 1 CASE (0121-1744-00) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (0121-1744-05) · 0121-1744-00
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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