NDC 72162-2195-01 - Bumetanide

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 72162-2195
Requested NDC: 72162-2195-01
Package NDCs from labels: 72162-2195-1, 72162-2195-01
Manufacturer: Bryant Ranch Prepack
Effective date: 2025-01-08
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Bumetanide - Bryant Ranch Prepack	Bryant Ranch Prepack	2025-01-08	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
72162-2195-1	Bumetanide	100 in 1 BOTTLE	TABLET	100		102

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72162-2195	BUMETANIDE TABLET [BRYANT RANCH PREPACK]	102	Current NDC, 1 package rows	20250110_80fe034e-01b7-438e-8378-44fafb7a1d94.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
72162-2195-1	EA - Each	72162-2195	3522dfa8-cae4-4b74-ae95-d21ccafa9a59	1	2024-01-04

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 5 of 5 · 83 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Bumetanide	BUMETANIDE	Novadoz Pharmaceuticals LLC	387edfd4-be85-41cd-8a6d-14e6a022b5a9	2022-08-09	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: 0Y2S3XUQ5H
Bumetanide	BUMETANIDE	Gland Pharma Limited	4d1ed6b2-c410-4f52-9b8a-aa256c37089e	2022-06-01	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: 0Y2S3XUQ5H
Bumetanide	BUMETANIDE	Aphena Pharma Solutions - Tennessee, LLC	7e47e7b1-d28a-4e12-882f-cf193b7f2697	2019-09-30	Boxed warning, Warnings, Adverse reactions	Exact identifier application number: ANDA074700 rxcui: 197418 unii: 0Y2S3XUQ5H

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.