Package 50090-6138-2

Brand: bumetanide

Generic: bumetanide
NDC Package

Package Facts

Identity

Package NDC 50090-6138-2
Digits Only 5009061382
Product NDC 50090-6138
Description

90 TABLET in 1 BOTTLE (50090-6138-2)

Marketing

Marketing Status
Marketed Since 2022-10-03
Brand bumetanide
Generic bumetanide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4529df9b-a34b-44ed-a1d1-03928d85db5e", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["197418"], "spl_set_id": ["cf29e436-b630-4b03-bb9b-9267ae77dc00"], "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 (50090-6138-2)", "package_ndc": "50090-6138-2", "marketing_start_date": "20221003"}], "brand_name": "bumetanide", "product_id": "50090-6138_4529df9b-a34b-44ed-a1d1-03928d85db5e", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "50090-6138", "generic_name": "bumetanide", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "bumetanide", "active_ingredients": [{"name": "BUMETANIDE", "strength": "1 mg/1"}], "application_number": "ANDA202900", "marketing_category": "ANDA", "marketing_start_date": "20180501", "listing_expiration_date": "20261231"}