Package 0832-0542-10

Brand: bumetanide

Generic: bumetanide
NDC Package

Package Facts

Identity

Package NDC 0832-0542-10
Digits Only 0832054210
Product NDC 0832-0542
Description

1000 TABLET in 1 BOTTLE (0832-0542-10)

Marketing

Marketing Status
Discontinued 2026-09-30
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": "d53166d9-64ca-4b76-81a7-b70a60c53b12", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0308320540115", "0308320541112"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["197417", "197418", "197419"], "spl_set_id": ["ff5dc8c6-b2f2-41d3-8e56-a953aa721b59"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Upsher-Smith Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (0832-0542-10)", "package_ndc": "0832-0542-10", "marketing_end_date": "20260930", "marketing_start_date": "20180130"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (0832-0542-11)", "package_ndc": "0832-0542-11", "marketing_end_date": "20260930", "marketing_start_date": "20180130"}], "brand_name": "Bumetanide", "product_id": "0832-0542_d53166d9-64ca-4b76-81a7-b70a60c53b12", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "0832-0542", "generic_name": "BUMETANIDE", "labeler_name": "Upsher-Smith Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bumetanide", "active_ingredients": [{"name": "BUMETANIDE", "strength": "2 mg/1"}], "application_number": "ANDA209916", "marketing_category": "ANDA", "marketing_end_date": "20260930", "marketing_start_date": "20180130"}