RecallHawk

METHOTREXATE SODIUM

AMNEAL PHARMS

Summary

FDA approved METHOTREXATE SODIUM by AMNEAL PHARMS. ANDA (Generic) approval (Labeling) on 2026-05-27. TABLET, ORAL.

Details

Source

Drug Approval

External ID

ANDA210040-15

Action Date

2026-05-27

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

METHOTREXATE SODIUM, TABLET, ORAL. Application: ANDA210040

Context & Analysis

AMNEAL PHARMS has 43 FDA actions in our database.

Frequently Asked Questions

How often does AMNEAL PHARMS have FDA actions?

AMNEAL PHARMS has 43 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 "ANDA210040-15" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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