Package 50090-7704-1
Brand: furosemide
Generic: furosemidePackage Facts
Identity
Package NDC
50090-7704-1
Digits Only
5009077041
Product NDC
50090-7704
Description
180 TABLET in 1 BOTTLE (50090-7704-1)
Marketing
Marketing Status
Brand
furosemide
Generic
furosemide
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1839739b-7e49-4a30-8305-a32ae079735a", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["313988"], "spl_set_id": ["c81d313c-65a3-4fb5-b6cd-b1c1ec7dca03"], "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 (50090-7704-1)", "package_ndc": "50090-7704-1", "marketing_start_date": "20251014"}], "brand_name": "Furosemide", "product_id": "50090-7704_1839739b-7e49-4a30-8305-a32ae079735a", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "50090-7704", "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": "ANDA078010", "marketing_category": "ANDA", "marketing_start_date": "20240603", "listing_expiration_date": "20261231"}