Home NDC 0074-0282 DECNUPAZ
Product NDC 0074-0282
11-digit product format 000740282
Labeler code 0074
Product ID 0074-0282_a7f31acd-4120-420a-ab5d-10415866e41a
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name pivekimab sunirine-pvzy
Dosage form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route INTRAVENOUS
Labeler AbbVie Inc.
Application BLA761460
Marketing category BLA
Marketing start 2026-05-27
Substance PIVEKIMAB SUNIRINE
Active strength 2 mg/mL
Listing certified through 2027-12-31
Current FDA listing Yes openFDA label cross-check# Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Additional Listing Data#
Finished product Yes
Brand name base DECNUPAZ
Listing expiration 2027-12-31
Active Ingredients# Ingredient, Strength table Ingredient Strength PIVEKIMAB SUNIRINE 2 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination L15LO3W1XX Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2744303 Internal RxNorm lookup 2744309 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# Purple Book Biologic Products# BLA, Proprietary name, Proper name table BLA Proprietary name Proper name License type Status Latest source 761460 Decnupaz pivekimab sunirine-pvzy 351(a) Rx 2026-06-01
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Status 0074-0282-02 00074028202 1 VIAL, SINGLE-DOSE in 1 CARTON (0074-0282-02) / 1.15 mL in 1 VIAL, SINGLE-DOSE 2026-05-27 0 Current