Package 68016-550-50

Brand: mucus relief dm

Generic: dextromethorphan hbr and guaifenesin
NDC Package

Package Facts

Identity

Package NDC 68016-550-50
Digits Only 6801655050
Product NDC 68016-550
Description

1 BOTTLE, PLASTIC in 1 CARTON (68016-550-50) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Discontinued 2026-03-31
Brand mucus relief dm
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": "7f4ceccf-ca96-4590-8910-0178e7a3de11", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0840986037702"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1147685"], "spl_set_id": ["9e32e9a9-b378-4f1d-82c4-c1769954fc10"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Chain Drug Consortium"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (68016-550-50)  / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "68016-550-50", "marketing_end_date": "20260331", "marketing_start_date": "20230112"}], "brand_name": "Mucus Relief DM", "product_id": "68016-550_7f4ceccf-ca96-4590-8910-0178e7a3de11", "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": "68016-550", "generic_name": "Dextromethorphan HBr and Guaifenesin", "labeler_name": "Chain Drug Consortium", "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_end_date": "20260331", "marketing_start_date": "20230112"}