Package 50090-7876-0

Brand: bumetanide

Generic: bumetanide
NDC Package

Package Facts

Identity

Package NDC 50090-7876-0
Digits Only 5009078760
Product NDC 50090-7876
Description

90 TABLET in 1 BOTTLE (50090-7876-0)

Marketing

Marketing Status
Marketed Since 2026-02-02
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": "3f0a567c-3d3a-46a9-9864-04eea0dd46ec", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["197419"], "spl_set_id": ["b338ae20-fc07-4ec5-9e68-be636f75ce1a"], "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": "90 TABLET in 1 BOTTLE (50090-7876-0)", "package_ndc": "50090-7876-0", "marketing_start_date": "20260202"}], "brand_name": "Bumetanide", "product_id": "50090-7876_3f0a567c-3d3a-46a9-9864-04eea0dd46ec", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "50090-7876", "generic_name": "Bumetanide", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bumetanide", "active_ingredients": [{"name": "BUMETANIDE", "strength": "2 mg/1"}], "application_number": "ANDA212931", "marketing_category": "ANDA", "marketing_start_date": "20250301", "listing_expiration_date": "20271231"}