Package 71335-2670-1

{"route": ["ORAL"], "spl_id": "0a28ab32-2722-4ba5-a18d-7a2b18a9e15f", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["197418"], "spl_set_id": ["a7068f36-a863-4af0-9c82-e5394a6e7a54"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (71335-2670-1)", "package_ndc": "71335-2670-1", "marketing_start_date": "20250626"}], "brand_name": "Bumetanide", "product_id": "71335-2670_0a28ab32-2722-4ba5-a18d-7a2b18a9e15f", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "71335-2670", "generic_name": "Bumetanide", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bumetanide", "active_ingredients": [{"name": "BUMETANIDE", "strength": "1 mg/1"}], "application_number": "ANDA074700", "marketing_category": "ANDA", "marketing_start_date": "19961121", "listing_expiration_date": "20261231"}