RecallHawk

PREGABALIN

ZYDUS PHARMS

Summary

FDA approved PREGABALIN by ZYDUS PHARMS. ANDA (Generic) approval (Labeling) on 2024-08-23. CAPSULE, ORAL.

Details

Source

Drug Approval

External ID

ANDA206752-3

Action Date

2024-08-23

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

PREGABALIN, CAPSULE, ORAL. Application: ANDA206752

Context & Analysis

ZYDUS PHARMS has 60 FDA actions in our database.

Frequently Asked Questions

How often does ZYDUS PHARMS have FDA actions?

ZYDUS PHARMS has 60 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 "ANDA206752-3" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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