Home NDC 55513-100-99 TEZSPIRE
Product NDC 55513-100
Requested package NDC 55513-100-99
11-digit product format 555130100
Labeler code 55513
Product ID 55513-100_25a4a901-927c-4f3a-a1c4-72826d46e946
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name tezepelumab-ekko
Dosage form INJECTION, SOLUTION
Route SUBCUTANEOUS
Labeler Amgen, Inc
Application BLA761224
Marketing category BLA
Marketing start 2021-12-17
Marketing end 0000-00-00
Substance TEZEPELUMAB
Active strength 210 mg/1.9mL
NDC exclude flag No
Listing certified through 2023-12-31
Current FDA listing Historical FDA.report record 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 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 55513-100 55513-100-99 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 55513-100 55513-100-99 D Discontinued by firm excluded / ndc_excluded.zip f5e01cc5f278…a2eaf40c39c3…
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 55513-100-01 TEZSPIRE 1.91 mL in 1 VIAL, GLASS INJECTION, SOLUTION 1.91 15 55513-100-01 TEZSPIRE 1 in 1 CARTON INJECTION, SOLUTION 1 15 55513-100-96 TEZSPIRE 1.91 mL in 1 VIAL, GLASS INJECTION, SOLUTION 1.91 15 55513-100-96 TEZSPIRE 1 in 1 CARTON INJECTION, SOLUTION 1 15 55513-100-99 TEZSPIRE 1.91 mL in 1 VIAL, GLASS INJECTION, SOLUTION 1.91 15
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 55513-100 TEZSPIRE (TEZEPELUMAB-EKKO) INJECTION, SOLUTION [AMGEN, INC] 10 Legacy NDC, 5 package rows 20240130_60f0aa03-ad25-4d48-80ce-7fcfa76f325f.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 761224 Tezspire tezepelumab-ekko 351(a) Rx 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 55513-100-99 55513010099 1.91 mL in 1 VIAL, GLASS (55513-100-99) 1.91 ml 2021-12-17 0000-00-00 Yes No Current