RecallHawk

DORZOLAMIDE HYDROCHLORIDE

FDC LTD

Summary

FDA approved DORZOLAMIDE HYDROCHLORIDE by FDC LTD. ANDA (Generic) approval (Labeling) on 2026-06-10. SOLUTION/DROPS, OPHTHALMIC.

Details

Source

Drug Approval

External ID

ANDA205294-8

Action Date

2026-06-10

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

DORZOLAMIDE HYDROCHLORIDE, SOLUTION/DROPS, OPHTHALMIC. Application: ANDA205294

Company

Context & Analysis

FDC LTD has 5 FDA actions in our database.

Frequently Asked Questions

How often does FDC LTD have FDA actions?

FDC LTD has 5 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 "ANDA205294-8" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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