Package 72854-157-20
Brand: mucinex fast-max severe congestion and cough
Generic: dextromethorphan hydrobromide, guaifenesinPackage Facts
Identity
Package NDC
72854-157-20
Digits Only
7285415720
Product NDC
72854-157
Description
2 BLISTER PACK in 1 CARTON (72854-157-20) / 10 TABLET, COATED in 1 BLISTER PACK
Marketing
Marketing Status
Brand
mucinex fast-max severe congestion and cough
Generic
dextromethorphan hydrobromide, guaifenesin
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3270eb5e-e724-609d-e063-6394a90ada8b", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0363824998558"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["2173726"], "spl_set_id": ["3270f369-7a40-186d-e063-6394a90a8526"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["RB Health (US) LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (72854-157-20) / 10 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "72854-157-20", "marketing_start_date": "20250701"}], "brand_name": "Mucinex Fast-Max Severe Congestion and Cough", "product_id": "72854-157_3270eb5e-e724-609d-e063-6394a90ada8b", "dosage_form": "TABLET, COATED", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]", "Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]"], "product_ndc": "72854-157", "generic_name": "Dextromethorphan hydrobromide, Guaifenesin", "labeler_name": "RB Health (US) LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucinex Fast-Max", "brand_name_suffix": "Severe Congestion and Cough", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "10 mg/1"}, {"name": "GUAIFENESIN", "strength": "200 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250701", "listing_expiration_date": "20261231"}