RecallHawk

MYCOPHENOLATE MOFETIL

ALKEM LABS LTD

Summary

FDA approved MYCOPHENOLATE MOFETIL by ALKEM LABS LTD. ANDA (Generic) approval (REMS) on 2024-08-13. TABLET, ORAL.

Details

Source

Drug Approval

External ID

ANDA091249-30

Action Date

2024-08-13

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

MYCOPHENOLATE MOFETIL, TABLET, ORAL. Application: ANDA091249

Context & Analysis

ALKEM LABS LTD has 50 FDA actions in our database.

Frequently Asked Questions

How often does ALKEM LABS LTD have FDA actions?

ALKEM LABS LTD has 50 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 "ANDA091249-30" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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