RecallHawk

Summary

FDA approved MICAFUNGIN by TEVA PHARMS USA INC. NDA (New Drug) approval (Type 5 - New Formulation or New Manufacturer) on 2021-07-30. POWDER, INTRAVENOUS.

Details

Source

Drug Approval

External ID

NDA212125-1

Action Date

2021-07-30

Status

Approved

Category

drug

Product Code

NDA (New Drug)

Product Description

MICAFUNGIN, POWDER, INTRAVENOUS. Application: NDA212125

Context & Analysis

TEVA PHARMS USA INC has 7 FDA actions in our database.

Frequently Asked Questions

How often does TEVA PHARMS USA INC have FDA actions?

TEVA PHARMS USA INC has 7 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 "NDA212125-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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