Package 72162-2195-1

Brand: bumetanide

Generic: bumetanide
NDC Package

Package Facts

Identity

Package NDC 72162-2195-1
Digits Only 7216221951
Product NDC 72162-2195
Description

100 TABLET in 1 BOTTLE (72162-2195-1)

Marketing

Marketing Status
Marketed Since 2023-12-15
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": "e56e97d2-919d-41e7-8a5b-a244bddcb3cb", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["197417"], "spl_set_id": ["80fe034e-01b7-438e-8378-44fafb7a1d94"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-2195-1)", "package_ndc": "72162-2195-1", "marketing_start_date": "20231215"}], "brand_name": "Bumetanide", "product_id": "72162-2195_e56e97d2-919d-41e7-8a5b-a244bddcb3cb", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "72162-2195", "generic_name": "Bumetanide", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bumetanide", "active_ingredients": [{"name": "BUMETANIDE", "strength": ".5 mg/1"}], "application_number": "ANDA074700", "marketing_category": "ANDA", "marketing_start_date": "19961121", "listing_expiration_date": "20261231"}