Package 0363-0533-32
Brand: mucus relief dm
Generic: dextromethorphan hbr, guaifenesinPackage Facts
Identity
Package NDC
0363-0533-32
Digits Only
0363053332
Product NDC
0363-0533
Description
2 BOTTLE, PLASTIC in 1 CARTON (0363-0533-32) / 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Marketing
Marketing Status
Brand
mucus relief dm
Generic
dextromethorphan hbr, guaifenesin
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8dece8a8-2f8b-4210-b1b6-2710092ab968", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0311917055121"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1147685"], "spl_set_id": ["cad5da8c-65a6-44c4-a4c7-38f2c7fe43aa"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Walgreen Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (0363-0533-01) / 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "0363-0533-01", "marketing_start_date": "20051231"}, {"sample": false, "description": "2 BOTTLE, PLASTIC in 1 CARTON (0363-0533-32) / 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "0363-0533-32", "marketing_start_date": "20051231"}], "brand_name": "Mucus Relief DM", "product_id": "0363-0533_8dece8a8-2f8b-4210-b1b6-2710092ab968", "dosage_form": "TABLET, FILM 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": "0363-0533", "generic_name": "Dextromethorphan HBr, Guaifenesin", "labeler_name": "Walgreen Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief DM", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/1"}, {"name": "GUAIFENESIN", "strength": "400 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20051231", "listing_expiration_date": "20261231"}