NDC 0517-1071 - Epinephrine

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: 0517-1071
Package NDCs from labels: 0517-1071-25
Manufacturer: American Regent, Inc.
Effective date: 2011-08-28
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
EPINEPHRINE INJECTION, USP	American Regent, Inc.	2011-08-28	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0517-1071-25	ML - Milliliter	0517-1071	96b8474d-85e8-483c-8b9d-5e4dc77a1cc0	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
EPINEPHRINE	ACTIVE INGREDIENT	YKH834O4BH	EPINEPHRINE INJECTION, SOLUTION [AMERICAN REGENT, INC.]	1
EPINEPHRINE	ACTIVE MOIETY	YKH834O4BH	EPINEPHRINE INJECTION, SOLUTION [AMERICAN REGENT, INC.]	1
HYDROCHLORIC ACID	INACTIVE INGREDIENT	QTT17582CB	EPINEPHRINE INJECTION, SOLUTION [AMERICAN REGENT, INC.]	1
SODIUM CHLORIDE	INACTIVE INGREDIENT	451W47IQ8X	EPINEPHRINE INJECTION, SOLUTION [AMERICAN REGENT, INC.]	1
SODIUM HYDROXIDE	INACTIVE INGREDIENT	55X04QC32I	EPINEPHRINE INJECTION, SOLUTION [AMERICAN REGENT, INC.]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	EPINEPHRINE INJECTION, SOLUTION [AMERICAN REGENT, INC.]	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 63 of 63 · 1,242 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Ringers	SODIUM CHLORIDE, CALCIUM CHLORIDE, POTASSIUM CHLORIDE,	Baxter Healthcare Corporation	e1953d54-818d-46a6-8532-518ebae6d84e	2012-06-13		Exact identifier unii: 451W47IQ8X
Lactated Ringers	SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE	Baxter Healthcare Corporation	f09f80bf-2f8b-4420-865d-aec2d5e5cd4d	2012-06-12		Exact identifier unii: 451W47IQ8X

Reported adverse events (FAERS/openFDA)#

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