Package 0641-6008-10

{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "99d2fc38-7e1e-4209-aa57-089794eda8a6", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["282486", "1727569"], "spl_set_id": ["681b5e9d-e2c7-4f29-aaad-e06d4a528c11"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (0641-6008-10)  / 4 mL in 1 VIAL (0641-6008-01)", "package_ndc": "0641-6008-10", "marketing_start_date": "20080430"}], "brand_name": "Bumetanide", "product_id": "0641-6008_99d2fc38-7e1e-4209-aa57-089794eda8a6", "dosage_form": "INJECTION", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "0641-6008", "generic_name": "Bumetanide", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bumetanide", "active_ingredients": [{"name": "BUMETANIDE", "strength": ".25 mg/mL"}], "application_number": "ANDA079196", "marketing_category": "ANDA", "marketing_start_date": "20080430", "listing_expiration_date": "20261231"}