Package 71335-2920-1

Brand: bumetanide

Generic: bumetanide
NDC Package

Package Facts

Identity

Package NDC 71335-2920-1
Digits Only 7133529201
Product NDC 71335-2920
Product ID 71335-2920_6472c7dd-189f-4816-b77a-3819ce5d649e
Description

500 TABLET in 1 BOTTLE (71335-2920-1)

Marketing

Marketing Status
Marketed Since 2025-10-21
Brand bumetanide
Generic bumetanide
Sample Package No

Linked Drug Pages (1)

Bumetanide ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "6472c7dd-189f-4816-b77a-3819ce5d649e", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["197418"], "spl_set_id": ["b2dcdf9b-70b9-493f-99b4-fc7dcc31939a"], "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": "500 TABLET in 1 BOTTLE (71335-2920-1)", "package_ndc": "71335-2920-1", "marketing_start_date": "20251021"}], "brand_name": "Bumetanide", "product_id": "71335-2920_6472c7dd-189f-4816-b77a-3819ce5d649e", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "71335-2920", "generic_name": "Bumetanide", "labeler_name": "Bryant Ranch Prepack", "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"}