RecallHawk

TIMOLOL MALEATE

SOMERSET

Summary

FDA approved TIMOLOL MALEATE by SOMERSET. ANDA (Generic) approval on 2024-07-03. SOLUTION/DROPS, OPHTHALMIC.

Details

Source

Drug Approval

External ID

ANDA217764-1

Action Date

2024-07-03

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

TIMOLOL MALEATE, SOLUTION/DROPS, OPHTHALMIC. Application: ANDA217764

Company

Context & Analysis

SOMERSET has 10 FDA actions in our database.

Frequently Asked Questions

How often does SOMERSET have FDA actions?

SOMERSET has 10 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 "ANDA217764-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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