Package 51655-517-52

{"route": ["ORAL"], "spl_id": "48e6d0b8-4a9a-74de-e063-6394a90ae680", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["310429", "313988"], "spl_set_id": ["1d99e151-75ba-6a75-e063-6294a90a4360"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (51655-517-26)", "package_ndc": "51655-517-26", "marketing_start_date": "20220711"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-517-52)", "package_ndc": "51655-517-52", "marketing_start_date": "20220624"}], "brand_name": "FUROSEMIDE", "product_id": "51655-517_48e6d0b8-4a9a-74de-e063-6394a90ae680", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "51655-517", "generic_name": "furosemide", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FUROSEMIDE", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "40 mg/1"}], "application_number": "ANDA077293", "marketing_category": "ANDA", "marketing_start_date": "20220624", "listing_expiration_date": "20271231"}