Package 50090-6647-1

{"route": ["ORAL"], "spl_id": "90d603f7-b6ec-4b86-b36f-8fc17d848e00", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["313988"], "spl_set_id": ["6194face-c26c-46ed-bde7-1e29bfeabd88"], "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": "180 TABLET in 1 BOTTLE (50090-6647-1)", "package_ndc": "50090-6647-1", "marketing_start_date": "20230829"}], "brand_name": "Furosemide", "product_id": "50090-6647_90d603f7-b6ec-4b86-b36f-8fc17d848e00", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "50090-6647", "generic_name": "Furosemide", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "40 mg/1"}], "application_number": "ANDA216629", "marketing_category": "ANDA", "marketing_start_date": "20221105", "listing_expiration_date": "20261231"}