RecallHawk

LOTEPREDNOL ETABONATE

SENTISS

Summary

FDA approved LOTEPREDNOL ETABONATE by SENTISS. ANDA (Generic) approval (Labeling) on 2025-01-28. GEL, OPHTHALMIC.

Details

Source

Drug Approval

External ID

ANDA212080-4

Action Date

2025-01-28

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

LOTEPREDNOL ETABONATE, GEL, OPHTHALMIC. Application: ANDA212080

Company

Context & Analysis

SENTISS has 2 FDA actions in our database.

Frequently Asked Questions

How often does SENTISS have FDA actions?

SENTISS has 2 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 "ANDA212080-4" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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