NDC 10019-180-05 - Enlon-Plus

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: 10019-180
Requested NDC: 10019-180-05
Package NDCs from labels: 10019-180-05
Manufacturer: Baxter Healthcare Corporation
Effective date: 2006-03-09
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Enlon-Plus - Baxter Healthcare Corporation	Baxter Healthcare Corporation	2006-03-09	HUMAN PRESCRIPTION DRUG LABELING

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
atropine sulfate	ACTIVE INGREDIENT	03J5ZE7KA5	ENLON-PLUS (EDROPHONIUM CHLORIDE AND ATROPINE SULFATE) INJECTION [BAXTER HEALTHCARE CORPORATION]	1
edrophonium chloride	ACTIVE INGREDIENT	QO611KSM5P	ENLON-PLUS (EDROPHONIUM CHLORIDE AND ATROPINE SULFATE) INJECTION [BAXTER HEALTHCARE CORPORATION]	1
atropine	ACTIVE MOIETY	7C0697DR9I	ENLON-PLUS (EDROPHONIUM CHLORIDE AND ATROPINE SULFATE) INJECTION [BAXTER HEALTHCARE CORPORATION]	1
edrophonium	ACTIVE MOIETY		ENLON-PLUS (EDROPHONIUM CHLORIDE AND ATROPINE SULFATE) INJECTION [BAXTER HEALTHCARE CORPORATION]	1
citric acid	INACTIVE INGREDIENT	2968PHW8QP	ENLON-PLUS (EDROPHONIUM CHLORIDE AND ATROPINE SULFATE) INJECTION [BAXTER HEALTHCARE CORPORATION]	1
phenol	INACTIVE INGREDIENT	339NCG44TV	ENLON-PLUS (EDROPHONIUM CHLORIDE AND ATROPINE SULFATE) INJECTION [BAXTER HEALTHCARE CORPORATION]	1
sodium citrate	INACTIVE INGREDIENT	1Q73Q2JULR	ENLON-PLUS (EDROPHONIUM CHLORIDE AND ATROPINE SULFATE) INJECTION [BAXTER HEALTHCARE CORPORATION]	1
sodium sulfite	INACTIVE INGREDIENT	VTK01UQK3G	ENLON-PLUS (EDROPHONIUM CHLORIDE AND ATROPINE SULFATE) 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
8D60A454-72C5-A9B8-D13F-B211813E35AC			bdeb47eb-e538-498d-ae98-14d5db29eab0	2006-03-09	Warnings, Adverse reactions	Exact identifier spl id: 8D60A454-72C5-A9B8-D13F-B211813E35AC spl set id: bdeb47eb-e538-498d-ae98-14d5db29eab0

Reported adverse events (FAERS/openFDA)#

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