NDC 0121-1775 – Guaifenesin and Codeine Phosphate

Guaifenesin 100 mg/5mL; Codeine Phosphate 10 mg/5mL · Solution · Oral

Human Otc Drug DEA schedule CV 1 recall

Product NDC0121-1775

Product details

Brand name
Guaifenesin and Codeine Phosphate
Generic name
Guaifenesin and Codeine Phosphate
Labeler
PAI Holdings, LLC
Dosage form
Solution
Route
Oral
Marketing category
OTC MONOGRAPH DRUG · M012
Marketed since
October 1, 2006
Listing expires
December 31, 2026
Pharmacologic class
Expectorant; Opioid Agonist

Active ingredients

Uses, dosage, side effects and warnings for Guaifenesin and Codeine Phosphate →

Package NDC codes (3)

Package NDCDescriptionSince
0121-1775-0010 TRAY in 1 CASE (0121-1775-00) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (0121-1775-05)Oct 1, 2006
0121-1775-1010 TRAY in 1 CASE (0121-1775-10) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSEOct 1, 2006
0121-1775-404 TRAY in 1 CASE (0121-1775-40) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (0121-1775-05)Jan 10, 2024

Recalls mentioning this NDC

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