RecallHawk

Summary

FDA approved BORTEZOMIB by PHARMASCIENCE INC. ANDA (Generic) approval on 2022-05-02. INJECTABLE, INTRAVENOUS, SUBCUTANEOUS.

Details

Source

Drug Approval

External ID

ANDA208392-1

Action Date

2022-05-02

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

BORTEZOMIB, INJECTABLE, INTRAVENOUS, SUBCUTANEOUS. Application: ANDA208392

Context & Analysis

Frequently Asked Questions

How often does PHARMASCIENCE INC have FDA actions?

This is the only FDA action we have on record for PHARMASCIENCE INC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "ANDA208392-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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