RecallHawk

AFINITOR DISPERZ (EVEROLIMUS)

NOVARTIS PHARM

Summary

FDA approved AFINITOR DISPERZ (EVEROLIMUS) by NOVARTIS PHARM. NDA (New Drug) approval (Labeling) on 2026-06-01. TABLET, FOR SUSPENSION, ORAL.

Details

Source

Drug Approval

External ID

NDA203985-28

Action Date

2026-06-01

Status

Approved

Category

drug

Product Code

NDA (New Drug)

Product Description

AFINITOR DISPERZ (generic: EVEROLIMUS), TABLET, FOR SUSPENSION, ORAL. Application: NDA203985

Context & Analysis

NOVARTIS PHARM has 2 FDA actions in our database.

Frequently Asked Questions

How often does NOVARTIS PHARM have FDA actions?

NOVARTIS PHARM has 2 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 "NDA203985-28" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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