United States · FDA National Drug Code directory
Guaifenesin and Codeine Phosphate
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
- 0121-1775_2175415b-f07e-50a6-e063-6394a90acabe
- Product NDC
- 0121-1775
- Form
- SOLUTION
- Composition / generic term
- Guaifenesin and Codeine Phosphate
- Labeler
- PAI Holdings, LLC
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20061001
- Source listing expiry
- 20261231
Source-listed ingredients
- GUAIFENESIN — 100 mg/5mL
- CODEINE PHOSPHATE — 10 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 TRAY in 1 CASE (0121-1775-00) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (0121-1775-05) · 0121-1775-00
- 10 TRAY in 1 CASE (0121-1775-10) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE · 0121-1775-10
- 4 TRAY in 1 CASE (0121-1775-40) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (0121-1775-05) · 0121-1775-40
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 →