Package 80425-0093-1

{"route": ["ORAL"], "spl_id": "2a996b2b-b5d6-65e7-e063-6394a90adeed", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["200371"], "spl_set_id": ["b3541f26-dc8d-6591-e053-2995a90a23d9"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (80425-0093-1)", "package_ndc": "80425-0093-1", "marketing_start_date": "20071018"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (80425-0093-2)", "package_ndc": "80425-0093-2", "marketing_start_date": "20071018"}], "brand_name": "Citalopram", "product_id": "80425-0093_2a996b2b-b5d6-65e7-e063-6394a90adeed", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "80425-0093", "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": "20 mg/1"}], "application_number": "ANDA078216", "marketing_category": "ANDA", "marketing_start_date": "20071018", "listing_expiration_date": "20261231"}