ACUVUE THERAVISION WITH KETOTIFEN
Summary
FDA approved ACUVUE THERAVISION WITH KETOTIFEN by JOHNSON JOHNSON VISN. NDA (New Drug) approval (Type 3 - New Dosage Form and Type 4 - New Combination) on 2022-02-25. DRUG-ELUTING CONTACT LENS, OPHTHALMIC.
Details
Source
Drug Approval
External ID
NDA022388-1
Action Date
2022-02-25
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
ACUVUE THERAVISION WITH KETOTIFEN, DRUG-ELUTING CONTACT LENS, OPHTHALMIC. Application: NDA022388
Company
Context & Analysis
Frequently Asked Questions
How often does JOHNSON JOHNSON VISN have FDA actions?
This is the only FDA action we have on record for JOHNSON JOHNSON VISN in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "NDA022388-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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