Package 76282-798-05

Brand: bumetanide

Generic: bumetanide
NDC Package

Package Facts

Identity

Package NDC 76282-798-05
Digits Only 7628279805
Product NDC 76282-798
Description

500 TABLET in 1 BOTTLE (76282-798-05)

Marketing

Marketing Status
Marketed Since 2025-03-01
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": "04a4ac27-f6b7-4a88-899b-93a5a21ddb6e", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0376282798059", "0376282797014", "0376282798011", "0376282799056", "0376282799018"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["197417", "197418", "197419"], "spl_set_id": ["06745425-e7e7-4413-b9ff-22b121f0ea9a"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Exelan Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (76282-798-01)", "package_ndc": "76282-798-01", "marketing_start_date": "20250301"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (76282-798-05)", "package_ndc": "76282-798-05", "marketing_start_date": "20250301"}], "brand_name": "Bumetanide", "product_id": "76282-798_04a4ac27-f6b7-4a88-899b-93a5a21ddb6e", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "76282-798", "generic_name": "Bumetanide", "labeler_name": "Exelan Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bumetanide", "active_ingredients": [{"name": "BUMETANIDE", "strength": "1 mg/1"}], "application_number": "ANDA212931", "marketing_category": "ANDA", "marketing_start_date": "20250301", "listing_expiration_date": "20271231"}