NDC 57926-465-01 - Salix

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: 57926-465
Requested NDC: 57926-465-01
Package NDCs from labels: 57926-465-01
Manufacturer: Merck Sharp & Dohme Corp.
Effective date: 2024-11-15
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
SALIX ® (furosemide injection)	Merck Sharp & Dohme Corp.	2024-11-15	PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
57926-465-01	Salix	1 in 1 CARTON	INJECTION	1		5
57926-465-01	Salix	50 mL in 1 VIAL, MULTI-DOSE	INJECTION	50		5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
57926-465	SALIX (FUROSEMIDE) INJECTION [MERCK SHARP & DOHME CORP.]	5	2 package rows	20241120_c3ff7e14-8232-40df-a5c8-60f98f5c1025.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Furosemide	ACTIVE INGREDIENT	7LXU5N7ZO5	SALIX (FUROSEMIDE) INJECTION [MERCK SHARP & DOHME CORP.]	2
Furosemide	ACTIVE MOIETY	7LXU5N7ZO5	SALIX (FUROSEMIDE) INJECTION [MERCK SHARP & DOHME CORP.]	2
Diethanolamine	INACTIVE INGREDIENT	AZE05TDV2V	SALIX (FUROSEMIDE) INJECTION [MERCK SHARP & DOHME CORP.]	2
Edetate Disodium	INACTIVE INGREDIENT	7FLD91C86K	SALIX (FUROSEMIDE) INJECTION [MERCK SHARP & DOHME CORP.]	2
Hydrochloric Acid	INACTIVE INGREDIENT	QTT17582CB	SALIX (FUROSEMIDE) INJECTION [MERCK SHARP & DOHME CORP.]	2
Nitrogen	INACTIVE INGREDIENT	N762921K75	SALIX (FUROSEMIDE) INJECTION [MERCK SHARP & DOHME CORP.]	2
Sodium Chloride	INACTIVE INGREDIENT	451W47IQ8X	SALIX (FUROSEMIDE) INJECTION [MERCK SHARP & DOHME CORP.]	2
Sodium Hydroxide	INACTIVE INGREDIENT	55X04QC32I	SALIX (FUROSEMIDE) INJECTION [MERCK SHARP & DOHME CORP.]	2
Sodium Sulfite	INACTIVE INGREDIENT	VTK01UQK3G	SALIX (FUROSEMIDE) INJECTION [MERCK SHARP & DOHME CORP.]	2
Water	INACTIVE INGREDIENT	059QF0KO0R	SALIX (FUROSEMIDE) INJECTION [MERCK SHARP & DOHME CORP.]	2

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 8 of 8 · 144 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Furosemide	FUROSEMIDE	Proficient Rx LP	ce84359c-2f76-421a-9b2b-79b1c2be2f20	2021-01-01	Warnings, Adverse reactions	Exact identifier unii: 7LXU5N7ZO5
Furosemide	FUROSEMIDE	Gland Pharma Limited	644704c0-e6a5-4804-bfa6-795c8f83aa7a	2020-07-03	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: 7LXU5N7ZO5
Furosemide	FUROSEMIDE	Aphena Pharma Solutions - Tennessee, LLC	1d2733ac-6fa6-44d1-96d4-f1a698045ad2	2018-04-18	Warnings, Adverse reactions	Exact identifier unii: 7LXU5N7ZO5
Furosemide	FUROSEMIDE	Aphena Pharma Solutions - Tennessee, LLC	6fbf7f3d-7566-44d5-9507-c4460238fc91	2018-02-09	Warnings, Adverse reactions	Exact identifier unii: 7LXU5N7ZO5

Reported adverse events (FAERS/openFDA)#

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