Home NDC 64193-425 FEIBA
Product NDC 64193-425
11-digit product format 641930425
Labeler code 64193
Product ID 64193-425_30be11d8-bb0b-4f10-8ef6-be656d679390
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name anti-inhibitor coagulant complex
Dosage form KIT
Labeler Takeda Pharmaceuticals America, Inc.
Application BLA101447
Marketing category BLA
Marketing start 1986-01-31
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes openFDA label cross-check# Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join FEIBA ANTI-INHIBITOR COAGULANT COMPLEX Takeda Pharmaceuticals America, Inc. 752604e5-4ea2-44f4-83ed-1569373f6412 2025-11-27 Boxed warning, Warnings, Adverse reactions Exact identifier application number: BLA101447 ndc (product): 64193-425
Additional Listing Data#
Finished product Yes
Brand name base FEIBA
Listing expiration 2026-12-31 Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1659998 Internal RxNorm lookup 1660001 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 64193-325-01 FEIBA 50 mL in 1 VIAL, GLASS POWDER, FOR SOLUTION 50 mL 2500 U in 50mL 30 64193-425-02 FEIBA 1 in 1 CARTON KIT 1 30
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 64193-425 FEIBA (ANTI-INHIBITOR COAGULANT COMPLEX) KIT [TAKEDA PHARMACEUTICALS AMERICA, INC.] 29 Current NDC, Legacy NDC, 2 package rows 20250109_752604e5-4ea2-44f4-83ed-1569373f6412.zip
Purple Book Biologic Products# BLA, Proprietary name, Proper name table BLA Proprietary name Proper name License type Status Latest source 101447 Autoplex, Feiba Nf, Feiba Vh Anti-Inhibitor Coagulant Complex 351(a) Disc 2026-06-01
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 64193-325-01 64193032501 50 mL in 1 VIAL, GLASS 50 ml Historical 64193-425-02 64193042502 1 KIT in 1 CARTON (64193-425-02) * 50 mL in 1 VIAL, GLASS (64193-325-01) * 50 mL in 1 VIAL, GLASS (64764-519-50) 1 kit 1986-01-31 0000-00-00 No No Current