Package 70000-0278-1

{"route": ["ORAL"], "spl_id": "63b596e2-a30f-4587-86ed-f0fc724b2f7e", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0096295131802"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1147685"], "spl_set_id": ["6304a581-9238-4539-b157-293fc05c173e"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Cardinal Health 110, LLC. DBA Leader"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (70000-0278-1)  / 12 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "70000-0278-1", "marketing_start_date": "20051231"}], "brand_name": "Mucus Relief DM Cough Maximum Strength", "product_id": "70000-0278_63b596e2-a30f-4587-86ed-f0fc724b2f7e", "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": "70000-0278", "generic_name": "Dextromethorphan HBr and Guaifenesin", "labeler_name": "Cardinal Health 110, LLC. DBA Leader", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief DM Cough", "brand_name_suffix": "Maximum Strength", "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"}