NDC 76489-001-01 - HemaCord

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: 76489-001
Requested NDC: 76489-001-01
Package NDCs from labels: 76489-001-01, 76489-001-02
Manufacturer: New York Blood Center | New York Blood Center, Inc.
Effective date: 2022-10-19
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
HemaCord - New York Blood Center \| New York Blood Center, Inc.	New York Blood Center \| New York Blood Center, Inc.	2022-10-19	CELLULAR THERAPY

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
76489-001-02	2025-01-30	C162847	48780-1	2cef2736-6f55-d83d-e063-dadaa90ab31f	These highlights do not include all the information needed to use HEMACORD safely and effectively. See full prescribing information for HEMACORD. HEMACORD (HPC, Cord Blood) Injectable Suspension for Intravenous Use Initial U.S. Approval: 2011

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
76489-001-01	HemaCord	25 mL in 1 BAG	INJECTION	25		9
76489-001-02	HemaCord	1 in 1 CANISTER	INJECTION	1		9

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
76489-001	HEMACORD (HUMAN CORD BLOOD HEMATOPOIETIC PROGENITOR CELL) INJECTION [NEW YORK BLOOD CENTER]	9	Legacy NDC, 2 package rows	20221020_bd9a5180-1773-11e0-980a-0002a5d5c51b.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
HUMAN CORD BLOOD HEMATOPOIETIC PROGENITOR CELL	ACTIVE INGREDIENT	XU53VK93MC	HEMACORD (HUMAN CORD BLOOD HEMATOPOIETIC PROGENITOR CELL) INJECTION [NEW YORK BLOOD CENTER]	5
HUMAN CORD BLOOD HEMATOPOIETIC PROGENITOR CELL	ACTIVE MOIETY	XU53VK93MC	HEMACORD (HUMAN CORD BLOOD HEMATOPOIETIC PROGENITOR CELL) INJECTION [NEW YORK BLOOD CENTER]	5
DIMETHYL SULFOXIDE	INACTIVE INGREDIENT	YOW8V9698H	HEMACORD (HUMAN CORD BLOOD HEMATOPOIETIC PROGENITOR CELL) INJECTION [NEW YORK BLOOD CENTER]	5

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 · 3 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Dimethyl Sulfoxide	DIMETHYL SULFOXIDE	Renova Pharmaceuticals LLC	8f699de6-9d09-48da-9d95-4001d7008587	2026-07-20	Warnings, Adverse reactions	Exact identifier unii: YOW8V9698H
eb63d261-e74f-f8fa-e053-2a95a90a538a			bd9a5180-1773-11e0-980a-0002a5d5c51b	2022-10-19	Boxed warning, Warnings, Adverse reactions	Exact identifier spl id: eb63d261-e74f-f8fa-e053-2a95a90a538a spl set id: bd9a5180-1773-11e0-980a-0002a5d5c51b
RIMSO-50	DIMETHYL SULFOXIDE	Mylan Institutional LLC	58b25d79-78f2-4953-b0c6-61658dc4ef0d	2021-03-17	Warnings, Adverse reactions	Exact identifier unii: YOW8V9698H

Reported adverse events (FAERS/openFDA)#

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