RecallHawk

POLIVY (POLATUZUMAB VEDOTIN)

GENENTECH

Summary

FDA approved POLIVY (POLATUZUMAB VEDOTIN) by GENENTECH. BLA (Biologic) approval (Labeling) on 2026-03-18. POWDER, INTRAVENOUS.

Details

Source

Drug Approval

External ID

BLA761121-17

Action Date

2026-03-18

Status

Approved

Category

drug

Product Code

BLA (Biologic)

Product Description

POLIVY (generic: POLATUZUMAB VEDOTIN), POWDER, INTRAVENOUS. Application: BLA761121

Company

Context & Analysis

GENENTECH has 6 FDA actions in our database.

Frequently Asked Questions

How often does GENENTECH have FDA actions?

GENENTECH has 6 FDA actions in our database, including 0 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "BLA761121-17" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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