Package 80425-0557-1

{"route": ["ORAL"], "spl_id": "43408cc0-4400-3827-e063-6394a90adcfe", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["283672"], "spl_set_id": ["434094b4-fa3b-385a-e063-6394a90ac638"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (80425-0557-1)", "package_ndc": "80425-0557-1", "marketing_start_date": "20251107"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (80425-0557-2)", "package_ndc": "80425-0557-2", "marketing_start_date": "20251107"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (80425-0557-3)", "package_ndc": "80425-0557-3", "marketing_start_date": "20251107"}], "brand_name": "Citalopram", "product_id": "80425-0557_43408cc0-4400-3827-e063-6394a90adcfe", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "80425-0557", "generic_name": "Citalopram", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "10 mg/1"}], "application_number": "ANDA078216", "marketing_category": "ANDA", "marketing_start_date": "20251107", "listing_expiration_date": "20261231"}