Home NDC 63459-305 HERZUMA
Product NDC 63459-305
11-digit product format 634590305
Labeler code 63459
Product ID 63459-305_49f6182a-5e0f-45ea-8a0f-b774ef28a98f
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name TRASTUZUMAB
Dosage form KIT
Labeler Cephalon, Inc.
Application BLA761091
Marketing category BLA
Marketing start 2020-03-16
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base HERZUMA
Listing expiration 2026-12-31 Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination P188ANX8CK Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 4 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2107053 Internal RxNorm lookup 2107058 Internal RxNorm lookup 2169359 Internal RxNorm lookup 2169362 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63459-305-47 HERZUMA 1 in 1 CARTON KIT 1 14 63459-307-41 HERZUMA 50 mL in 1 VIAL, MULTI-DOSE INJECTION, POWDER, LYOPHILIZED, 50 mL 420 mg in 20mL 14
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 63459-305 HERZUMA (TRASTUZUMAB) KIT HERZUMA (TRASTUZUMAB) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [CEPHALON, INC.] 13 Current NDC, Legacy NDC, 2 package rows 20250419_ae71c003-883a-4cd8-ad50-e8cc9a54e971.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.
Purple Book Biologic Products# BLA, Proprietary name, Proper name table BLA Proprietary name Proper name License type Status Latest source 761091 Herzuma trastuzumab-pkrb 351(k) Biosimilar Rx 2026-07-01
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 63459-305-47 63459030547 1 KIT in 1 CARTON (63459-305-47) * 50 mL in 1 VIAL, MULTI-DOSE (63459-307-41) * 20 mL in 1 VIAL (63459-221-20) 1 kit 2020-03-16 0000-00-00 No No Current 63459-307-41 63459030741 50 mL in 1 VIAL, MULTI-DOSE 50 ml Historical