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OLOPATADINE HYDROCHLORIDE OPHTHALMIC SOLUTION

BAUSCH AND LOMB INC

Summary

FDA approved OLOPATADINE HYDROCHLORIDE OPHTHALMIC SOLUTION by BAUSCH AND LOMB INC. ANDA (Generic) approval (Manufacturing (CMC)) on 2024-08-07. SOLUTION/DROPS, OPHTHALMIC.

Details

Source

Drug Approval

External ID

ANDA206046-3

Action Date

2024-08-07

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

OLOPATADINE HYDROCHLORIDE OPHTHALMIC SOLUTION, SOLUTION/DROPS, OPHTHALMIC. Application: ANDA206046

Context & Analysis

BAUSCH AND LOMB INC has 5 FDA actions in our database.

Frequently Asked Questions

How often does BAUSCH AND LOMB INC have FDA actions?

BAUSCH AND LOMB INC 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 "ANDA206046-3" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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