NDC 10019-873-15 - ENLON

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: 10019-873
Requested NDC: 10019-873-15
Package NDCs from labels: 10019-873-39, 10019-873-15
Manufacturer: Baxter Healthcare Corporation
Effective date: 2006-10-17
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
ENLON - Baxter Healthcare Corporation	Baxter Healthcare Corporation	2006-10-17	HUMAN PRESCRIPTION DRUG LABELING

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
10019-873-15	ENLON	1 in 1 PACKAGE	INJECTION	1		1
10019-873-39	ENLON	15 mL in 1 VIAL	INJECTION	15		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
10019-873	ENLON (EDROPHONIUM CHLORIDE) INJECTION [BAXTER HEALTHCARE CORPORATION]	1	2 package rows	20061215_312042cf-df60-4dc5-90dd-4e77ebd4a781.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
edrophonium chloride	ACTIVE INGREDIENT	QO611KSM5P	ENLON (EDROPHONIUM CHLORIDE) INJECTION [BAXTER HEALTHCARE CORPORATION]	1
edrophonium cation	ACTIVE MOIETY	70FP3JLY7N	ENLON (EDROPHONIUM CHLORIDE) INJECTION [BAXTER HEALTHCARE CORPORATION]	1
citric acid	INACTIVE INGREDIENT	2968PHW8QP	ENLON (EDROPHONIUM CHLORIDE) INJECTION [BAXTER HEALTHCARE CORPORATION]	1
phenol	INACTIVE INGREDIENT	339NCG44TV	ENLON (EDROPHONIUM CHLORIDE) INJECTION [BAXTER HEALTHCARE CORPORATION]	1
sodium citrate	INACTIVE INGREDIENT	1Q73Q2JULR	ENLON (EDROPHONIUM CHLORIDE) INJECTION [BAXTER HEALTHCARE CORPORATION]	1
sodium sulfite	INACTIVE INGREDIENT	VTK01UQK3G	ENLON (EDROPHONIUM CHLORIDE) INJECTION [BAXTER HEALTHCARE CORPORATION]	1

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
312042cf-df60-4dc5-90dd-4e77ebd4a781			312042cf-df60-4dc5-90dd-4e77ebd4a781	2006-10-17	Warnings, Adverse reactions	Exact identifier spl id: 312042cf-df60-4dc5-90dd-4e77ebd4a781 spl set id: 312042cf-df60-4dc5-90dd-4e77ebd4a781

Reported adverse events (FAERS/openFDA)#

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