RecallHawk

BORTEZOMIB

SHUANGCHENG

Summary

FDA approved BORTEZOMIB by SHUANGCHENG. ANDA (Generic) approval on 2025-12-17. INJECTABLE, INTRAVENOUS, SUBCUTANEOUS.

Details

Source

Drug Approval

External ID

ANDA216528-1

Action Date

2025-12-17

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

BORTEZOMIB, INJECTABLE, INTRAVENOUS, SUBCUTANEOUS. Application: ANDA216528

Context & Analysis

SHUANGCHENG has 3 FDA actions in our database.

Frequently Asked Questions

How often does SHUANGCHENG have FDA actions?

SHUANGCHENG has 3 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 "ANDA216528-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

Want to know the moment something like this happens?

Get alerts for drug

Related Actions