Package 71205-804-90

{"route": ["ORAL"], "spl_id": "3f90b8dd-7234-4428-b896-943d052dd05f", "openfda": {"upc": ["0371205804305"], "unii": ["BKE5Q1J60U"], "rxcui": ["835593"], "spl_set_id": ["3f90b8dd-7234-4428-b896-943d052dd05f"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-804-30)", "package_ndc": "71205-804-30", "marketing_start_date": "20230605"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-804-60)", "package_ndc": "71205-804-60", "marketing_start_date": "20230605"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-804-90)", "package_ndc": "71205-804-90", "marketing_start_date": "20230605"}], "brand_name": "Imipramine Hydrochloride", "product_id": "71205-804_3f90b8dd-7234-4428-b896-943d052dd05f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "71205-804", "generic_name": "Imipramine Hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Imipramine Hydrochloride", "active_ingredients": [{"name": "IMIPRAMINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA040903", "marketing_category": "ANDA", "marketing_start_date": "20160407", "listing_expiration_date": "20261231"}