"72854-001-32" National Drug Code (NDC)

NDC Code	72854-001-32
Package Description	4 BLISTER PACK in 1 CARTON (72854-001-32) / 8 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC	72854-001
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Mucinex
Proprietary Name Suffix	12hr Cold And Fever Multi-symptom
Non-Proprietary Name	Naproxen Sodium, Dextromethorphan Hydrobromide, Guaifenesin
Dosage Form	TABLET, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20260601
Marketing Category Name	NDA
Application Number	NDA217338
Manufacturer	Reckitt Benckiser LLC
Substance Name	DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; NAPROXEN SODIUM
Strength	30; 600; 110
Strength Unit	mg/1; mg/1; mg/1
Pharmacy Classes	Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], Nonsteroidal Anti-inflammatory Drug [EPC], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA]