Package 70518-4387-0

Brand: bumetanide

Generic: bumetanide
NDC Package

Package Facts

Identity

Package NDC 70518-4387-0
Digits Only 7051843870
Product NDC 70518-4387
Product ID 70518-4387_3955d55c-b866-e166-e063-6394a90af1f6
Description

90 TABLET in 1 BOTTLE, PLASTIC (70518-4387-0)

Marketing

Marketing Status
Marketed Since 2025-07-06
Brand bumetanide
Generic bumetanide
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3955d55c-b866-e166-e063-6394a90af1f6", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["197419"], "spl_set_id": ["0fb78afc-d8bc-4ae8-8c0a-6d9c6f7a22c5"], "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 (70518-4387-0)", "package_ndc": "70518-4387-0", "marketing_start_date": "20250706"}], "brand_name": "Bumetanide", "product_id": "70518-4387_3955d55c-b866-e166-e063-6394a90af1f6", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "70518-4387", "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": "ANDA074700", "marketing_category": "ANDA", "marketing_start_date": "20250706", "listing_expiration_date": "20261231"}