RecallHawk

THIORIDAZINE HYDROCHLORIDE

PHARM ASSOC

Summary

FDA approved THIORIDAZINE HYDROCHLORIDE by PHARM ASSOC. ANDA (Generic) approval (Labeling) on 2025-01-22. CONCENTRATE, ORAL.

Details

Source

Drug Approval

External ID

ANDA040213-4

Action Date

2025-01-22

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

THIORIDAZINE HYDROCHLORIDE, CONCENTRATE, ORAL. Application: ANDA040213

Context & Analysis

PHARM ASSOC has 13 FDA actions in our database.

Frequently Asked Questions

How often does PHARM ASSOC have FDA actions?

PHARM ASSOC has 13 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 "ANDA040213-4" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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