NDC 51662-1441-01 - IRON 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: 51662-1441
Requested NDC: 51662-1441-01
Package NDCs from labels: 51662-1441-1, 51662-1441-01
Manufacturer: HF Acquisition Co LLC, DBA HealthFirst
Effective date: 2025-01-08
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
IRON DEXTRAN - HF Acquisition Co LLC, DBA HealthFirst	HF Acquisition Co LLC, DBA HealthFirst	2025-01-08	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
51662-1441-1	IRON DEXTRAN	2 mL in 1 VIAL, SINGLE-DOSE	INJECTION	2		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51662-1441	IRON DEXTRAN INJECTION [HF ACQUISITION CO LLC, DBA HEALTHFIRST]	3	Current NDC, Legacy NDC, 1 package rows	20250110_9a4cd424-865d-fdd1-e053-2995a90a00ff.zip

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 · 5 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
INFED	IRON DEXTRAN	Henry Schein, Inc.	99bf34be-cb8a-46d1-9637-5544dc2da287	2026-04-15	Boxed warning, Warnings, Adverse reactions	Exact identifier application number: NDA017441 rxcui: 206216 rxcui: 311144 unii: 95HR524N2M
Se-Tan PLUS	MULTIVITAMIN/MINERAL	Seton Pharmaceuticals	56e912df-3a49-4405-8df1-7b80d12bd920	2025-04-24	Boxed warning, Adverse reactions	Exact identifier unii: 95HR524N2M
IRON DEXTRAN	IRON DEXTRAN	HF Acquisition Co LLC, DBA HealthFirst	9a4cd424-865d-fdd1-e053-2995a90a00ff	2025-01-08	Boxed warning, Warnings, Adverse reactions	Exact identifier application number: NDA017441 ndc (package): 51662-1441-1 ndc (product): 51662-1441 ndc11 (package): 51662144101 rxcui: 311144 spl id: 2b3948f4-fdef-5321-e063-6394a90ad70c spl set id: 9a4cd424-865d-fdd1-e053-2995a90a00ff unii: 95HR524N2M
INFeD	IRON DEXTRAN	Allergan, Inc.	94b01b1e-794b-4bea-8e24-2e54683fc023	2024-08-02	Boxed warning, Warnings, Adverse reactions	Exact identifier application number: NDA017441 ndc (product): 0023-6082 rxcui: 206216 rxcui: 311144 spl id: d6b2a709-570d-4ceb-8772-7961d247a42b spl set id: 94b01b1e-794b-4bea-8e24-2e54683fc023 unii: 95HR524N2M
PureVit DualFe Plus	FERROUS FUMARATE, POLYSACCHARIDE IRON COMPLEX	PureTek Corporation	71f63741-cad4-43b5-bb3e-c63a188d10a2	2023-01-11	Warnings, Adverse reactions	Exact identifier unii: 95HR524N2M

Reported adverse events (FAERS/openFDA)#

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