Package 50844-633-11

Brand: mucus relief dm cough

Generic: dextromethorphan hbr and guaifenesin
NDC Package

Package Facts

Identity

Package NDC 50844-633-11
Digits Only 5084463311
Product NDC 50844-633
Description

1 BOTTLE, PLASTIC in 1 CARTON (50844-633-11) / 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2023-08-07
Brand mucus relief dm cough
Generic dextromethorphan hbr and guaifenesin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "661a2205-98b6-410a-970a-5712c7f192bd", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0350844633118"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1147685"], "spl_set_id": ["2fea3533-8218-4875-affe-5b33a22c553a"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["L.N.K. International, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (50844-633-11)  / 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "50844-633-11", "marketing_start_date": "20230807"}], "brand_name": "Mucus Relief DM Cough", "product_id": "50844-633_661a2205-98b6-410a-970a-5712c7f192bd", "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": "50844-633", "generic_name": "Dextromethorphan HBr and Guaifenesin", "labeler_name": "L.N.K. International, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief DM Cough", "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": "20230807", "listing_expiration_date": "20261231"}