Package 16571-678-01

{"route": ["ORAL"], "spl_id": "ad19edfb-a229-4767-890a-3bf6558ec191", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["197417", "197418", "197419"], "spl_set_id": ["627c9732-eed1-4435-8d79-2e19ab974fd9"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Rising Pharma Holdings, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (16571-678-01)", "package_ndc": "16571-678-01", "marketing_start_date": "20240603"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (16571-678-10)", "package_ndc": "16571-678-10", "marketing_start_date": "20240603"}], "brand_name": "Bumetanide", "product_id": "16571-678_ad19edfb-a229-4767-890a-3bf6558ec191", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "16571-678", "generic_name": "bumetanide", "labeler_name": "Rising Pharma Holdings, Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bumetanide", "active_ingredients": [{"name": "BUMETANIDE", "strength": "1 mg/1"}], "application_number": "ANDA212019", "marketing_category": "ANDA", "marketing_start_date": "20240603", "listing_expiration_date": "20261231"}