RecallHawk

Summary

FDA approved CABERGOLINE by IVAX SUB TEVA PHARMS. ANDA (Generic) approval (Labeling) on 2023-06-28. TABLET, ORAL.

Details

Source

Drug Approval

External ID

ANDA077750-11

Action Date

2023-06-28

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

CABERGOLINE, TABLET, ORAL. Application: ANDA077750

Context & Analysis

IVAX SUB TEVA PHARMS has 3 FDA actions in our database.

Frequently Asked Questions

How often does IVAX SUB TEVA PHARMS have FDA actions?

IVAX SUB TEVA PHARMS has 3 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 "ANDA077750-11" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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