RecallHawk

LATANOPROST

MICRO LABS

Summary

FDA approved LATANOPROST by MICRO LABS. ANDA (Generic) approval on 2025-04-14. SOLUTION/DROPS, OPHTHALMIC.

Details

Source

Drug Approval

External ID

ANDA219306-1

Action Date

2025-04-14

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

LATANOPROST, SOLUTION/DROPS, OPHTHALMIC. Application: ANDA219306

Company

Context & Analysis

MICRO LABS has 35 FDA actions in our database.

Frequently Asked Questions

How often does MICRO LABS have FDA actions?

MICRO LABS has 35 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 "ANDA219306-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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