Home NDC 85052-101 Trutakna
Product NDC 85052-101
11-digit product format 850520101
Labeler code 85052
Product ID 85052-101_83f672ee-5ed8-4226-aae7-16bb625f7088
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name atacicept
Dosage form INJECTION, SOLUTION
Route SUBCUTANEOUS
Labeler Vera Therapeutics, Inc
Application BLA761486
Marketing category BLA
Marketing start 2026-07-07
Substance ATACICEPT
Active strength 150 mg/1
Listing certified through 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Trutakna
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ATACICEPT 150 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination K3D9A0ICQ3 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2747237 Internal RxNorm lookup 2747244 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 761486 Trutakna atacicept-vymj 351(a) Rx 2026-08-01
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Status 85052-101-04 85052010104 4 SYRINGE, GLASS in 1 CARTON (85052-101-04) / 1 INJECTION, SOLUTION in 1 SYRINGE, GLASS (85052-101-01) 2026-07-07 0 Current