Package 50090-6345-2

Brand: bumetanide

Generic: bumetanide
NDC Package

Package Facts

Identity

Package NDC 50090-6345-2
Digits Only 5009063452
Product NDC 50090-6345
Description

90 TABLET in 1 BOTTLE (50090-6345-2)

Marketing

Marketing Status
Marketed Since 2023-01-24
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": "2b846551-7dac-40bf-bbed-29b20f760767", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["197418"], "spl_set_id": ["7f9dccf8-37ff-454b-9d55-7f1d631c8483"], "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 (50090-6345-2)", "package_ndc": "50090-6345-2", "marketing_start_date": "20230124"}], "brand_name": "Bumetanide", "product_id": "50090-6345_2b846551-7dac-40bf-bbed-29b20f760767", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "50090-6345", "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": "ANDA074700", "marketing_category": "ANDA", "marketing_start_date": "19961121", "listing_expiration_date": "20261231"}