Package 41226-280-03

{"route": ["ORAL"], "spl_id": "89697bdd-6c45-47bf-e053-2a95a90aa0ca", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1147685"], "spl_set_id": ["813baf42-edb0-33a9-e053-2a91aa0a8599"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["KROGER COMPANY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (41226-280-03)", "package_ndc": "41226-280-03", "marketing_start_date": "20190603"}], "brand_name": "MUCUS RELIEF DM", "product_id": "41226-280_89697bdd-6c45-47bf-e053-2a95a90aa0ca", "dosage_form": "TABLET", "pharm_class": ["Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]"], "product_ndc": "41226-280", "generic_name": "DEXTROMETHORPHAN HBR/GUAIFENESIN", "labeler_name": "KROGER 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": "part341", "marketing_category": "OTC MONOGRAPH FINAL", "marketing_start_date": "20190603", "listing_expiration_date": "20261231"}