RecallHawk

MYCOPHENOLATE MOFETIL

MEITHEAL

Summary

FDA approved MYCOPHENOLATE MOFETIL by MEITHEAL. ANDA (Generic) approval (REMS) on 2024-08-13. INJECTABLE, INJECTION.

Details

Source

Drug Approval

External ID

ANDA212130-10

Action Date

2024-08-13

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

MYCOPHENOLATE MOFETIL, INJECTABLE, INJECTION. Application: ANDA212130

Company

Context & Analysis

MEITHEAL has 26 FDA actions in our database.

Frequently Asked Questions

How often does MEITHEAL have FDA actions?

MEITHEAL has 26 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 "ANDA212130-10" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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