RecallHawk

PANRETIN (ALITRETINOIN)

ADVANZ PHARMA

Summary

FDA approved PANRETIN (ALITRETINOIN) by ADVANZ PHARMA. NDA (New Drug) approval (Labeling) on 2025-11-17. GEL, TOPICAL.

Details

Source

Drug Approval

External ID

NDA020886-9

Action Date

2025-11-17

Status

Approved

Category

drug

Product Code

NDA (New Drug)

Product Description

PANRETIN (generic: ALITRETINOIN), GEL, TOPICAL. Application: NDA020886

Context & Analysis

ADVANZ PHARMA has 2 FDA actions in our database.

Frequently Asked Questions

How often does ADVANZ PHARMA have FDA actions?

ADVANZ PHARMA 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 "NDA020886-9" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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