NDC 0121-1550 – Guaifenesin and Codeine Phosphate

Guaifenesin 200 mg/10mL; Codeine Phosphate 20 mg/10mL · Solution · Oral

Human Otc Drug DEA schedule CV 1 recall

Product NDC0121-1550

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 (2)

Package NDCDescriptionSince
0121-1550-0010 TRAY in 1 CASE (0121-1550-00) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (0121-1550-10)Oct 1, 2006
0121-1550-404 TRAY in 1 CASE (0121-1550-40) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (0121-1550-10)Jan 10, 2024

Recalls mentioning this NDC

Other Guaifenesin and Codeine Phosphate products