Guaifenesin and Codeine Phosphate

NDC 0121-1775 · PAI Holdings, LLC

Generic nameGuaifenesin and Codeine Phosphate

Dosage formSOLUTION

RouteORAL

Active ingredient(s)GUAIFENESIN, CODEINE PHOSPHATE

Strength10; 100 mg/5mL; mg/5mL

Pharmacologic classDecreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Full Opioid Agonists [MoA], Increased Respiratory Secretions [PE], Opioid Agonist [EPC]

DEA scheduleCV

Marketing categoryOTC MONOGRAPH DRUG

Packages

0121-1775-00 — 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)

0121-1775-10 — 10 TRAY in 1 CASE (0121-1775-10) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE

0121-1775-40 — 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)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0113-8911 — guaifenesin, pseudoephedrine hydrochloride, 0121-0504 — ACETAMINOPHEN and CODEINE PHOSPHATE, 0121-0638 — GUAIFENESIN and DEXTROMETHORPHAN, 0121-0744 — GUAIFENESIN, 0121-0775 — Guaifenesin and Codeine Phosphate, 0121-1008 — ACETAMINOPHEN and CODEINE PHOSPHATE, 0121-1276 — GUAIFENESIN and DEXTROMETHORPHAN, 0121-1488 — GUAIFENESIN, 0121-1550 — Guaifenesin and Codeine Phosphate, 0121-1744 — GUAIFENESIN, 0121-2232 — GUAIFENESIN, 0280-0061 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 0280-0089 — dextromethorphan hydrobromide, guaifenesin, 0280-0505 — Alka-Seltzer Plus Severe Cough Mucus and Congestion, 0280-0507 — Acetaminophen, Dextromethorphan hydrobromide, Guaifenesin, Phenylephrine hydrochloride, 0280-0921 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 0280-8273 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 0280-8294 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 0363-0028 — Guaifenesin, 0363-0033 — Guaifenesin, +1534 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.