RecallHawk

PAROXETINE

LEGACY PHARMA

Summary

FDA approved PAROXETINE by LEGACY PHARMA. NDA (New Drug) approval (Labeling) on 2025-02-11. CAPSULE, ORAL.

Details

Source

Drug Approval

External ID

NDA204516-9

Action Date

2025-02-11

Status

Approved

Category

drug

Product Code

NDA (New Drug)

Product Description

PAROXETINE, CAPSULE, ORAL. Application: NDA204516

Context & Analysis

LEGACY PHARMA has 2 FDA actions in our database.

Frequently Asked Questions

How often does LEGACY PHARMA have FDA actions?

LEGACY 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 "NDA204516-9" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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