ABBVIE INC: Biologic license for DECNUPAZ

ABBVIE INC: Biologic license for DECNUPAZ. Dated 161 days ago, it serves as a historical benchmark. Score 55/100. As of 2026-11-03, from openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration).

Data as of · Compiled by Zalwin from openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration)

Free preview: all 7 published fields of this record are shown below. Locked: 499 related FdaApprovalPulse records and the 4-column CSV export.

FieldValue
SponsorABBVIE INC
ProductDECNUPAZ
Generic / ingredientPIVEKIMAB SUNIRINE-PVZY
ApprovalBiologic license (BLA)
ApplicationBLA761460
Decided2026-05-27
Panel / classVIAL, SINGLE-DOSE
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  • Source agency: openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration)
  • Record date: 2026-05-27
  • Data refreshed: 2026-11-03
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LIVE PUBLIC DATA Source: openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration) · Last refreshed: Tue, 03 Nov 2026 05:14:00 GMT

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55 / 100 Score

  • A new product launch.

What is the FdaApprovalPulse record for ABBVIE INC?

The FDA approved DECNUPAZ (BLA761460) for ABBVIE INC on 2026-05-27: biologic license (BLA).

How does ABBVIE INC compare to other FdaApprovalPulse records?

It is 161 days old; check the official source for later updates before acting.

ABBVIE INC vs. top 3 peers

OrganizationRecord date
ABBVIE INC2026-05-27
AMGEN INC2026-10-22
SANDOZ INC2026-10-22
TEVA PHARMACEUTICALS, INC.2026-09-25

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From openFDA (PMA and Drugs@FDA). openFDA can lag FDA decisions by days to weeks. Drug supplement types follow the FDA submission class (labeling and REMS, manufacturing/CMC, efficacy, other). Company and product level only. Verify on FDA databases before relying on an approval.

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