NDC 58005-040-04 - IRON HYDROGENATED DEXTRAN

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: 58005-040
Requested NDC: 58005-040-04
Package NDCs from labels: 58005-040-04
Manufacturer: Sparhawk Laboratories, Inc.
Effective date: 2024-05-30
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
IRON HYDROGENATED DEXTRAN INJECTION	Sparhawk Laboratories, Inc.	2024-05-30	OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
58005-040-04	IRON HYDROGENATED DEXTRAN	100 mL in 1 VIAL	INJECTION	100		10

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
58005-040	IRON HYDROGENATED DEXTRAN (IRON) INJECTION [SPARHAWK LABORATORIES, INC.]	10	1 package rows	20240601_2dcbe68c-7297-4a78-948b-5e7c6b72cafc.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version	Uploaded
IRON	ACTIVE INGREDIENT	E1UOL152H7	IRON HYDROGENATED DEXTRAN (IRON) INJECTION [SPARHAWK LABORATORIES, INC.]	6
IRON	ACTIVE MOIETY	E1UOL152H7	IRON HYDROGENATED DEXTRAN (IRON) INJECTION [SPARHAWK LABORATORIES, INC.]	6

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 9 of 9 · 161 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Heavy Metal Detox T014	ALLIUM SATIVUM, AVENA SATIVA, BERBERIS VULGARIS, LAPPA MAJOR, PHYTOLACCA DECANDRA, SOLIDAGO VIRGAUREA, LYCOPODIUM CLAVATUM, NUX VOMICA, ALUMINUM METALLICUM, ANTIMONIUM CRUDUM, ARGENTUM METALLICUM, ARSENICUM ALBUM, AURUM METALLICUM, BARYTA CARBONICA, BERYLLIUM METALLICUM, BISMUTHUM METALLICUM, BORON, BROMIUM, CADMIUM METALLICUM, CERIUM METALLICUM, CESIUM CHLORIDE, CHROMIUM, COBALTUM METALLICUM, CUPRUM METALLICUM, DYSPROSIUM METALLICUM, ERBIUM METALLICUM, EUROPIUM METALLICUM, FERRUM METALLICUM	Guangzhou Renuma Medical Systems Co., Ltd	41ce8009-71f2-418c-a38d-0cfaccfb74b4	2017-10-26	Warnings	Exact identifier unii: E1UOL152H7

Reported adverse events (FAERS/openFDA)#

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