Package 50090-7736-0

{"route": ["ORAL"], "spl_id": "1f7a9bc7-10d5-47eb-90b4-a68968996d04", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["197417"], "spl_set_id": ["14e92f79-2c7b-4ab9-844f-e7bd1964f8b2"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7736-0)", "package_ndc": "50090-7736-0", "marketing_start_date": "20251028"}], "brand_name": "Bumetanide", "product_id": "50090-7736_1f7a9bc7-10d5-47eb-90b4-a68968996d04", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "50090-7736", "generic_name": "Bumetanide", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bumetanide", "active_ingredients": [{"name": "BUMETANIDE", "strength": ".5 mg/1"}], "application_number": "ANDA213942", "marketing_category": "ANDA", "marketing_start_date": "20250116", "listing_expiration_date": "20261231"}