Package 31722-368-32

{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "32ba5fc2-0f9e-ee77-e063-6294a90af010", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0331722369107"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["282486", "1727569"], "spl_set_id": ["084b34ad-36ba-43bd-a43a-1f4b4da26d8f"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (31722-368-32)  / 4 mL in 1 VIAL, SINGLE-DOSE (31722-368-31)", "package_ndc": "31722-368-32", "marketing_start_date": "20250227"}], "brand_name": "Bumetanide", "product_id": "31722-368_32ba5fc2-0f9e-ee77-e063-6294a90af010", "dosage_form": "INJECTION", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "31722-368", "generic_name": "Bumetanide", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bumetanide", "active_ingredients": [{"name": "BUMETANIDE", "strength": ".25 mg/mL"}], "application_number": "ANDA218746", "marketing_category": "ANDA", "marketing_start_date": "20250227", "listing_expiration_date": "20261231"}