RecallHawk

MYCOPHENOLATE MOFETIL HYDROCHLORIDE

AMNEAL

Summary

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

Details

Source

Drug Approval

External ID

ANDA211374-8

Action Date

2024-08-13

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

MYCOPHENOLATE MOFETIL HYDROCHLORIDE, INJECTABLE, INJECTION. Application: ANDA211374

Company

Context & Analysis

AMNEAL has 70 FDA actions in our database.

Frequently Asked Questions

How often does AMNEAL have FDA actions?

AMNEAL has 70 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 "ANDA211374-8" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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