Package 11673-235-66

{"route": ["ORAL"], "spl_id": "617ebd8b-85db-4a79-a9b3-877f77ffa75b", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1099074"], "spl_set_id": ["5bcb49ee-94c2-4624-824a-84213ab152b1"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (11673-235-30)  / 28 TABLET, EXTENDED RELEASE in 1 BOTTLE", "package_ndc": "11673-235-30", "marketing_start_date": "20180927"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (11673-235-55)  / 42 TABLET, EXTENDED RELEASE in 1 BOTTLE", "package_ndc": "11673-235-55", "marketing_start_date": "20200417"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (11673-235-66)  / 14 TABLET, EXTENDED RELEASE in 1 BOTTLE", "package_ndc": "11673-235-66", "marketing_start_date": "20180927"}], "brand_name": "up and up maximum strength mucus relief dm", "product_id": "11673-235_617ebd8b-85db-4a79-a9b3-877f77ffa75b", "dosage_form": "TABLET, EXTENDED RELEASE", "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": "11673-235", "generic_name": "dextromethorphan hydrobromide, guaifenesin", "labeler_name": "Target Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "up and up maximum strength mucus relief dm", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "60 mg/1"}, {"name": "GUAIFENESIN", "strength": "1200 mg/1"}], "application_number": "ANDA207602", "marketing_category": "ANDA", "marketing_start_date": "20180927", "listing_expiration_date": "20261231"}