Package 50090-5664-0

Brand: bumetanide

Generic: bumetanide
NDC Package

Package Facts

Identity

Package NDC 50090-5664-0
Digits Only 5009056640
Product NDC 50090-5664
Description

90 TABLET in 1 BOTTLE (50090-5664-0)

Marketing

Marketing Status
Marketed Since 2021-09-15
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": "1b3acb4a-bcb0-42d5-8600-6bf02fcc06c0", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["197417"], "spl_set_id": ["f4326e53-5217-48d4-a089-1184442049ac"], "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 (50090-5664-0)", "package_ndc": "50090-5664-0", "marketing_start_date": "20210915"}], "brand_name": "Bumetanide", "product_id": "50090-5664_1b3acb4a-bcb0-42d5-8600-6bf02fcc06c0", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "50090-5664", "generic_name": "Bumetanide", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bumetanide", "active_ingredients": [{"name": "BUMETANIDE", "strength": ".5 mg/1"}], "application_number": "ANDA209724", "marketing_category": "ANDA", "marketing_start_date": "20171018", "listing_expiration_date": "20271231"}