RecallHawk

EVOMELA (MELPHALAN)

ACROTECH BIOPHARMA

Summary

FDA approved EVOMELA (MELPHALAN) by ACROTECH BIOPHARMA. NDA (New Drug) approval (Labeling) on 2022-04-26. POWDER, INTRAVENOUS.

Details

Source

Drug Approval

External ID

NDA207155-5

Action Date

2022-04-26

Status

Approved

Category

drug

Product Code

NDA (New Drug)

Product Description

EVOMELA (generic: MELPHALAN), POWDER, INTRAVENOUS. Application: NDA207155

Context & Analysis

Frequently Asked Questions

How often does ACROTECH BIOPHARMA have FDA actions?

This is the only FDA action we have on record for ACROTECH BIOPHARMA in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "NDA207155-5" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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