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 Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
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
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 · 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
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 2026-09-01
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