NDC 64764-517 - FEIBA

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: 64764-517
Package NDCs from labels: 64764-517-20
Manufacturer: Takeda Pharmaceuticals America, Inc. | Takeda Manufacturing Austria AG | Siegfried Hameln GmbH
Effective date: 2025-11-27
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
FEIBA - Takeda Pharmaceuticals America, Inc. \| Takeda Manufacturing Austria AG \| Siegfried Hameln GmbH	Takeda Pharmaceuticals America, Inc. \| Takeda Manufacturing Austria AG \| Siegfried Hameln GmbH	2025-11-27	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
64764-517	FEIBA (ANTI-INHIBITOR COAGULANT COMPLEX) KIT [TAKEDA PHARMACEUTICALS AMERICA, INC.]	29	Unmatched	20250109_752604e5-4ea2-44f4-83ed-1569373f6412.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
ANTI-INHIBITOR COAGULANT COMPLEX	ACTIVE INGREDIENT	CS849DUN3M	FEIBA NF (ANTI-INHIBITOR COAGULANT COMPLEX) KIT [BAXTER HEALTHCARE CORPORATION]	7
ANTI-INHIBITOR COAGULANT COMPLEX	ACTIVE MOIETY	CS849DUN3M	FEIBA NF (ANTI-INHIBITOR COAGULANT COMPLEX) KIT [BAXTER HEALTHCARE CORPORATION]	7
SODIUM CHLORIDE	INACTIVE INGREDIENT	451W47IQ8X	FEIBA NF (ANTI-INHIBITOR COAGULANT COMPLEX) KIT [BAXTER HEALTHCARE CORPORATION]	7
TRISODIUM CITRATE DIHYDRATE	INACTIVE INGREDIENT	B22547B95K	FEIBA NF (ANTI-INHIBITOR COAGULANT COMPLEX) KIT [BAXTER HEALTHCARE CORPORATION]	7
Water	INACTIVE INGREDIENT	059QF0KO0R	FEIBA NF (ANTI-INHIBITOR COAGULANT COMPLEX) KIT [BAXTER HEALTHCARE CORPORATION]	7

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 51 of 51 · 1,003 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Join
TIS-U-SOL	SODIUM CHLORIDE, POTASSIUM CHLORIDE, MAGNESIUM SULFATE, SODIUM PHOSPHATE, AND POTASSIUM PHOSPHATE	Baxter Healthcare Corporation	9da4121f-d62d-4da4-8dfb-0494da16015f	2014-02-21	Exact identifier unii: 451W47IQ8X
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.