TYRVAYA (VARENICLINE)
Summary
FDA approved TYRVAYA (VARENICLINE) by OYSTER POINT PHARMA. NDA (New Drug) approval (Labeling) on 2024-02-02. SPRAY, NASAL.
Details
Source
Drug Approval
External ID
NDA213978-5
Action Date
2024-02-02
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
TYRVAYA (generic: VARENICLINE), SPRAY, NASAL. Application: NDA213978
Company
Context & Analysis
Frequently Asked Questions
How often does OYSTER POINT PHARMA have FDA actions?
This is the only FDA action we have on record for OYSTER POINT PHARMA in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "NDA213978-5" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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