RecallHawk

KETOROLAC TROMETHAMINE

EUGIA PHARMA

Summary

FDA approved KETOROLAC TROMETHAMINE by EUGIA PHARMA. ANDA (Generic) approval (Labeling) on 2024-03-29. SOLUTION/DROPS, OPHTHALMIC.

Details

Source

Drug Approval

External ID

ANDA205191-2

Action Date

2024-03-29

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

KETOROLAC TROMETHAMINE, SOLUTION/DROPS, OPHTHALMIC. Application: ANDA205191

Context & Analysis

EUGIA PHARMA has 44 FDA actions in our database.

Frequently Asked Questions

How often does EUGIA PHARMA have FDA actions?

EUGIA PHARMA has 44 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 "ANDA205191-2" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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