Home NDC 51759-709 Ustekinumab-aekn
Product NDC 51759-709
11-digit product format 517590709
Labeler code 51759
Product ID 51759-709_1577b43b-65ee-4da4-9821-338d1651d3d7
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name ustekinumab-aekn
Dosage form INJECTION, SOLUTION
Route SUBCUTANEOUS
Labeler Teva Pharmaceuticals USA, Inc.
Application BLA761343
Marketing category BLA
Marketing start 2025-06-02
Substance USTEKINUMAB-AEKN
Active strength 45 mg/.5mL
Pharmacologic classes Interleukin-12 Antagonist [EPC], Interleukin-12 Antagonists [MoA], Interleukin-23 Antagonist [EPC], Interleukin-23 Antagonists [MoA]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 4 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 51759-709-32 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 51759-709-32 f5e01cc5f278…a2eaf40c39c3…
Additional Listing Data#
Finished product Yes
Brand name base Ustekinumab-aekn
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength USTEKINUMAB-AEKN 45 mg/.5mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination FU77B4U5Z0 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2705393 Internal RxNorm lookup 2705400 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 51759-709-32 Ustekinumab-aekn 1 in 1 CARTON INJECTION, SOLUTION 1 9 51759-709-32 Ustekinumab-aekn 1 in 1 TRAY INJECTION, SOLUTION 1 9
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 · 4 matching rows.
Purple Book Biologic Products# BLA, Proprietary name, Proper name table BLA Proprietary name Proper name License type Status Latest source 761343 Selarsdi ustekinumab-aekn 351(k) Interchangeable Rx 2026-07-01
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 51759-709-32 51759070932 1 TRAY in 1 CARTON (51759-709-32) / 1 SYRINGE, GLASS in 1 TRAY / .5 mL in 1 SYRINGE, GLASS 1 tray 2025-06-02 No No Current