Package 55301-533-01

Brand: mucus relief dm

Generic: dextromethorphan hbr and guaifenesin
NDC Package

Package Facts

Identity

Package NDC 55301-533-01
Digits Only 5530153301
Product NDC 55301-533
Description

3 BLISTER PACK in 1 CARTON (55301-533-01) / 10 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2005-12-31
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": "865f0d0f-c777-4d09-8db9-7580c003fff8", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0614299404397"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1147685"], "spl_set_id": ["dc0a3761-bbe2-4261-a183-594f5fb12b0b"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["ARMY AND AIR FORCE EXCHANGE SERVICE"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (55301-533-01)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "55301-533-01", "marketing_start_date": "20051231"}], "brand_name": "Mucus Relief DM", "product_id": "55301-533_865f0d0f-c777-4d09-8db9-7580c003fff8", "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": "55301-533", "generic_name": "Dextromethorphan HBr and Guaifenesin", "labeler_name": "ARMY AND AIR FORCE EXCHANGE SERVICE", "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"}