RecallHawk

GEFITINIB

NATCO

Summary

FDA approved GEFITINIB by NATCO. ANDA (Generic) approval on 2023-05-31. TABLET, ORAL.

Details

Source

Drug Approval

External ID

ANDA212827-1

Action Date

2023-05-31

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

GEFITINIB, TABLET, ORAL. Application: ANDA212827

Company

Context & Analysis

NATCO has 6 FDA actions in our database.

Frequently Asked Questions

How often does NATCO have FDA actions?

NATCO has 6 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 "ANDA212827-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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