RecallHawk

TRAZODONE HYDROCHLORIDE

CROSSMEDIKA SA

Summary

FDA approved TRAZODONE HYDROCHLORIDE by CROSSMEDIKA SA. ANDA (Generic) approval (Labeling) on 2025-06-24. TABLET, ORAL.

Details

Source

Drug Approval

External ID

ANDA211116-4

Action Date

2025-06-24

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

TRAZODONE HYDROCHLORIDE, TABLET, ORAL. Application: ANDA211116

Context & Analysis

CROSSMEDIKA SA has 2 FDA actions in our database.

Frequently Asked Questions

How often does CROSSMEDIKA SA have FDA actions?

CROSSMEDIKA SA 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 "ANDA211116-4" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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