RecallHawk

EVEROLIMUS

HIKMA

Summary

FDA approved EVEROLIMUS by HIKMA. ANDA (Generic) approval on 2021-11-23. TABLET, ORAL.

Details

Source

Drug Approval

External ID

ANDA207486-2

Action Date

2021-11-23

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

EVEROLIMUS, TABLET, ORAL. Application: ANDA207486

Company

Context & Analysis

HIKMA has 117 FDA actions in our database.

Frequently Asked Questions

How often does HIKMA have FDA actions?

HIKMA has 117 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 "ANDA207486-2" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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