Package 51672-4225-1

{"route": ["ORAL"], "spl_id": "18e97584-09e5-8246-e063-6294a90a8d93", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0351672422417"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["197417", "197418", "197419"], "spl_set_id": ["5c753aae-77b7-4add-8453-385a8f62d7db"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Taro Pharmaceuticals U.S.A., Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (51672-4225-1)", "package_ndc": "51672-4225-1", "marketing_start_date": "20230724"}], "brand_name": "Bumetanide", "product_id": "51672-4225_18e97584-09e5-8246-e063-6294a90a8d93", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "51672-4225", "generic_name": "Bumetanide", "labeler_name": "Taro Pharmaceuticals U.S.A., Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bumetanide", "active_ingredients": [{"name": "BUMETANIDE", "strength": "2 mg/1"}], "application_number": "ANDA213458", "marketing_category": "ANDA", "marketing_start_date": "20230724", "listing_expiration_date": "20261231"}