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Codeine-Guaifenesin

NDC 72162-1669 · Bryant Ranch Prepack

Generic nameCodeine Phosphate and Guaifenesin
Dosage formSOLUTION
RouteORAL
Active ingredient(s)CODEINE PHOSPHATE, GUAIFENESIN
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

72162-1669-2 — 120 mL in 1 BOTTLE (72162-1669-2)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72036-980 — Guaifenesin and Dextromethorphan HBr, 72090-009 — guaifenesin 400 mg, 72090-011 — Guaifenesin, 72090-012 — Guaifenesin, 72090-013 — guaifenesin 400 mg, 72090-019 — guaifenesin 400 mg, 72090-027 — Dextromethorphan HBr 20mg Guaifenesin 400mg, 72090-035 — guaifenesin 400 mg, 72090-044 — Guaifenesin 400 mg, 72162-1591 — Butalbital, Acetaminophen, Caffeine and Codeine Phosphate, 72162-2001 — acetaminophen and codeine phosphate, 72162-2002 — acetaminophen and codeine phosphate, 72162-2042 — Promethazine Hydrochloride and Codeine Phosphate, 72162-2277 — Guaifenesin and Dextromethorphan Hydrobromide, 72162-2278 — Guaifenesin, 72189-376 — Acetaminophen and Codeine Phosphate, 72288-219 — dextromethorphan hydrobromide, guaifenesin, 72288-220 — Guaifenesin and Dextromethorphan HBr, 72288-293 — Dextromethorphan HBr, Guaifenesin, 72288-298 — 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.