Package 0185-0129-05

{"route": ["ORAL"], "spl_id": "c6f31ac9-10d1-4d92-882e-836de10e1ce6", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0301850128013", "0301850129010", "0301850130016"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["197418", "197419", "197417"], "spl_set_id": ["05cb961d-ac33-4bcf-b04e-411e496c43c1"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0185-0129-01)", "package_ndc": "0185-0129-01", "marketing_start_date": "19961121"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (0185-0129-05)", "package_ndc": "0185-0129-05", "marketing_start_date": "19961121"}], "brand_name": "Bumetanide", "product_id": "0185-0129_c6f31ac9-10d1-4d92-882e-836de10e1ce6", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "0185-0129", "generic_name": "Bumetanide", "labeler_name": "Sandoz Inc", "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"}