United States · FDA National Drug Code directory
GUAIFENESIN - ODAAT 1200 MG
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
- 83139-175_f61d3ae0-11ec-2a82-e053-2995a90a95da
- Product NDC
- 83139-175
- Form
- TABLET
- Composition / generic term
- GUAIFENESIN
- Labeler
- LODAAT LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230304
- Source listing expiry
- 20261231
Source-listed ingredients
- GUAIFENESIN — 1200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (83139-175-01) · 83139-175-01
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 →