Package 82868-050-90

{"route": ["ORAL"], "spl_id": "476ccce7-7a09-d249-e063-6394a90a9af4", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["310429"], "spl_set_id": ["13ba97a7-598a-76a4-e063-6294a90a45c5"], "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": "30 TABLET in 1 BOTTLE, PLASTIC (82868-050-30)", "package_ndc": "82868-050-30", "marketing_start_date": "20240229"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (82868-050-90)", "package_ndc": "82868-050-90", "marketing_start_date": "20240229"}], "brand_name": "Furosemide", "product_id": "82868-050_476ccce7-7a09-d249-e063-6394a90a9af4", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "82868-050", "generic_name": "Furosemide", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "20 mg/1"}], "application_number": "ANDA216629", "marketing_category": "ANDA", "marketing_start_date": "20240229", "listing_expiration_date": "20271231"}