VARDENAFIL HYDROCHLORIDE
Summary
FDA approved VARDENAFIL HYDROCHLORIDE by CROSSMEDIKA SA. ANDA (Generic) approval (Labeling) on 2024-01-31. TABLET, ORAL.
Details
Source
Drug Approval
External ID
ANDA209057-5
Action Date
2024-01-31
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
VARDENAFIL HYDROCHLORIDE, TABLET, ORAL. Application: ANDA209057
Company
Context & Analysis
CROSSMEDIKA SA has 2 FDA actions in our database.
Frequently Asked Questions
How often does CROSSMEDIKA SA have FDA actions?
CROSSMEDIKA SA 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 "ANDA209057-5" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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