Package 63561-0165-2
Brand: furosemide
Generic: furosemidePackage Facts
Identity
Package NDC
63561-0165-2
Digits Only
6356101652
Product NDC
63561-0165
Description
1000 TABLET in 1 BOTTLE (63561-0165-2)
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": "4870846b-dfe5-84bd-e063-6294a90aa56f", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0363561016492", "0363561016423", "0363561016652", "0363561016515", "0363561016591", "0363561016522"], "unii": ["7LXU5N7ZO5"], "rxcui": ["197732", "310429", "313988"], "spl_set_id": ["462e8917-cbe0-f4f9-e063-6394a90ab4ff"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Granulation Technology, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (63561-0165-1)", "package_ndc": "63561-0165-1", "marketing_start_date": "20260115"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (63561-0165-2)", "package_ndc": "63561-0165-2", "marketing_start_date": "20251218"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (63561-0165-9)", "package_ndc": "63561-0165-9", "marketing_start_date": "20251218"}], "brand_name": "Furosemide", "product_id": "63561-0165_4870846b-dfe5-84bd-e063-6294a90aa56f", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "63561-0165", "generic_name": "FUROSEMIDE", "labeler_name": "Granulation Technology, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "40 mg/1"}], "application_number": "NDA018569", "marketing_category": "NDA", "marketing_start_date": "20251218", "listing_expiration_date": "20271231"}