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AMGEN INC: Biologic license for PAVBLU
AMGEN INC: Biologic license for PAVBLU. Dated 13 days ago, it is in the active follow-up window. Score 85/100. 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.
| Field | Value |
|---|---|
| Sponsor | AMGEN INC |
| Product | PAVBLU |
| Generic / ingredient | AFLIBERCEPT-AYYH |
| Approval | Biologic license (BLA) |
| Application | BLA761298 |
| Decided | 2026-10-22 |
| Panel / class | INJECTABLE, INJECTION |
| Peer records CSV (500 records) | 🔒 Click to unlock → |
| CRM-ready export with official source URLs | 🔒 Click to unlock → |
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CSV columns: Sponsor · Product · Approval · Decided · official source URL
- Source agency: openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration)
- Record date: 2026-10-22
- Data refreshed: 2026-11-03
- Refunds on request within 14 days
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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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85 / 100 Score
- Decided in the last 30 days.
- A new product launch.
What is the FdaApprovalPulse record for AMGEN INC?
The FDA approved PAVBLU (BLA761298) for AMGEN INC on 2026-10-22: biologic license (BLA).
How does AMGEN INC compare to other FdaApprovalPulse records?
It is fresh: dated 13 days ago, inside the window where early outreach matters most. Its Score of 85/100 puts it among the stronger signals in this feed.
AMGEN INC vs. top 3 peers
| Organization | Record date |
|---|---|
| AMGEN INC | 2026-10-22 |
| SANDOZ INC | 2026-10-22 |
| TEVA PHARMACEUTICALS, INC. | 2026-09-25 |
| ELI LILLY AND CO | 2026-09-23 |
Related records
FdaApprovalPulse: Biologic license (BLA)
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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.