Package 51662-1449-1

Brand: bumetanide

Generic: bumetanide
NDC Package

Package Facts

Identity

Package NDC 51662-1449-1
Digits Only 5166214491
Product NDC 51662-1449
Product ID 51662-1449_2b395f11-a2e3-6a43-e063-6394a90a4efa
Description

4 mL in 1 VIAL (51662-1449-1)

Marketing

Marketing Status
Marketed Since 2020-01-11
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": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "2b395f11-a2e3-6a43-e063-6394a90a4efa", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["1727569"], "spl_set_id": ["9bd7a71e-0e78-dae7-e053-2995a90ad110"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "4 mL in 1 VIAL (51662-1449-1)", "package_ndc": "51662-1449-1", "marketing_start_date": "20200111"}], "brand_name": "BUMETANIDE", "product_id": "51662-1449_2b395f11-a2e3-6a43-e063-6394a90a4efa", "dosage_form": "INJECTION", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "51662-1449", "generic_name": "BUMETANIDE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BUMETANIDE", "active_ingredients": [{"name": "BUMETANIDE", "strength": ".25 mg/mL"}], "application_number": "ANDA079196", "marketing_category": "ANDA", "marketing_start_date": "20200111", "listing_expiration_date": "20261231"}