LEVOCETIRIZINE DIHYDROCHLORIDE
Summary
FDA approved LEVOCETIRIZINE DIHYDROCHLORIDE by TEVA PHARMS. ANDA (Generic) approval (Labeling) on 2025-07-11. TABLET, ORAL.
Details
Source
Drug Approval
External ID
ANDA090199-22
Action Date
2025-07-11
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
LEVOCETIRIZINE DIHYDROCHLORIDE, TABLET, ORAL. Application: ANDA090199
Company
Context & Analysis
TEVA PHARMS has 14 FDA actions in our database.
Frequently Asked Questions
How often does TEVA PHARMS have FDA actions?
TEVA PHARMS has 14 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 "ANDA090199-22" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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