Package 69238-1491-5

{"route": ["ORAL"], "spl_id": "d1961e90-3fcc-4b72-b207-6c9de6d66557", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0369238149111", "0369238149012", "0369238148916"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["197417", "197418", "197419"], "spl_set_id": ["9188ab17-8539-48a5-905f-ad35ab5a0b93"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Amneal Pharmaceuticals NY LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (69238-1491-1)", "package_ndc": "69238-1491-1", "marketing_start_date": "20171018"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (69238-1491-5)", "package_ndc": "69238-1491-5", "marketing_start_date": "20171018"}], "brand_name": "Bumetanide", "product_id": "69238-1491_d1961e90-3fcc-4b72-b207-6c9de6d66557", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "69238-1491", "generic_name": "Bumetanide", "labeler_name": "Amneal Pharmaceuticals NY LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bumetanide", "active_ingredients": [{"name": "BUMETANIDE", "strength": "2 mg/1"}], "application_number": "ANDA209724", "marketing_category": "ANDA", "marketing_start_date": "20171018", "listing_expiration_date": "20261231"}