Package 70518-4478-0

Brand: bumetanide

Generic: bumetanide
NDC Package

Package Facts

Identity

Package NDC 70518-4478-0
Digits Only 7051844780
Product NDC 70518-4478
Description

90 TABLET in 1 BOTTLE, PLASTIC (70518-4478-0)

Marketing

Marketing Status
Marketed Since 2025-09-12
Brand bumetanide
Generic bumetanide
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3e9b97a1-21dc-4fbb-e063-6394a90afd8c", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["197419"], "spl_set_id": ["c5d87c7c-3d03-4a9a-8f07-382371c55169"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-4478-0)", "package_ndc": "70518-4478-0", "marketing_start_date": "20250912"}], "brand_name": "Bumetanide", "product_id": "70518-4478_3e9b97a1-21dc-4fbb-e063-6394a90afd8c", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "70518-4478", "generic_name": "Bumetanide", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bumetanide", "active_ingredients": [{"name": "BUMETANIDE", "strength": "2 mg/1"}], "application_number": "ANDA213942", "marketing_category": "ANDA", "marketing_start_date": "20250912", "listing_expiration_date": "20261231"}