RecallHawk

BORTEZOMIB

GLAND

Summary

FDA approved BORTEZOMIB by GLAND. ANDA (Generic) approval on 2026-01-06. POWDER, INTRAVENOUS, SUBCUTANEOUS.

Details

Source

Drug Approval

External ID

ANDA219167-1

Action Date

2026-01-06

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

BORTEZOMIB, POWDER, INTRAVENOUS, SUBCUTANEOUS. Application: ANDA219167

Company

Context & Analysis

GLAND has 40 FDA actions in our database.

Frequently Asked Questions

How often does GLAND have FDA actions?

GLAND has 40 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 "ANDA219167-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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