RecallHawk

QINLOCK (RIPRETINIB)

DECIPHERA PHARMS

Summary

FDA approved QINLOCK (RIPRETINIB) by DECIPHERA PHARMS. NDA (New Drug) approval (Labeling) on 2025-05-06. TABLET, ORAL.

Details

Source

Drug Approval

External ID

NDA213973-10

Action Date

2025-05-06

Status

Approved

Category

drug

Product Code

NDA (New Drug)

Product Description

QINLOCK (generic: RIPRETINIB), TABLET, ORAL. Application: NDA213973

Context & Analysis

DECIPHERA PHARMS has 2 FDA actions in our database.

Frequently Asked Questions

How often does DECIPHERA PHARMS have FDA actions?

DECIPHERA PHARMS 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 "NDA213973-10" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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