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

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.

Identifier, FDA.report destination table
Identifier	FDA.report destination
508b6ff8-601d-4901-a7a5-816141134054	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
0ca1d589-929b-4b33-bc5b-1d84abdafa6a	Product name	1	20150324
fc363c46-397b-4476-ac0f-70e43e8e4592	Product name	1	20150324

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.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
DECNUPAZ	PIVEKIMAB SUNIRINE-PVZY	AbbVie Inc.	508b6ff8-601d-4901-a7a5-816141134054	2026-05-27	Boxed warning, Warnings, Adverse reactions	Exact identifier application number: BLA761460 ndc (product): 0074-0282

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	2026-08-01

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