RecallHawk

CYCLOSPORINE

DEVA HOLDING AS

Summary

FDA approved CYCLOSPORINE by DEVA HOLDING AS. ANDA (Generic) approval on 2024-05-21. EMULSION, OPHTHALMIC.

Details

Source

Drug Approval

External ID

ANDA209811-1

Action Date

2024-05-21

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

CYCLOSPORINE, EMULSION, OPHTHALMIC. Application: ANDA209811

Context & Analysis

DEVA HOLDING AS has 7 FDA actions in our database.

Frequently Asked Questions

How often does DEVA HOLDING AS have FDA actions?

DEVA HOLDING AS has 7 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 "ANDA209811-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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