Package 69584-671-09

{"route": ["ORAL"], "spl_id": "2ac7f06f-af78-4705-a209-d9041b2de825", "openfda": {"unii": ["X2ELS050D8"], "rxcui": ["1738483", "1738495", "1738503", "1738511"], "spl_set_id": ["25182b68-8f7a-48e8-9788-6818b0984b29"], "manufacturer_name": ["Oxford Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (69584-671-03)", "package_ndc": "69584-671-03", "marketing_start_date": "20221114"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (69584-671-09)", "package_ndc": "69584-671-09", "marketing_start_date": "20221114"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (69584-671-10)", "package_ndc": "69584-671-10", "marketing_start_date": "20221114"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (69584-671-50)", "package_ndc": "69584-671-50", "marketing_start_date": "20221114"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (69584-671-90)", "package_ndc": "69584-671-90", "marketing_start_date": "20221114"}], "brand_name": "paroxetine hydrochloride", "product_id": "69584-671_2ac7f06f-af78-4705-a209-d9041b2de825", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "69584-671", "generic_name": "paroxetine hydrochloride", "labeler_name": "Oxford Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "paroxetine hydrochloride", "active_ingredients": [{"name": "PAROXETINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA076968", "marketing_category": "ANDA", "marketing_start_date": "20221114", "listing_expiration_date": "20261231"}