ALLERGY RELIEF (FEXOFENADINE HCL)
Summary
FDA approved ALLERGY RELIEF (FEXOFENADINE HCL) by GRANULES. ANDA (Generic) approval (Labeling) on 2024-01-04. TABLET, ORAL.
Details
Source
Drug Approval
External ID
ANDA211075-8
Action Date
2024-01-04
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
ALLERGY RELIEF (generic: FEXOFENADINE HCL), TABLET, ORAL. Application: ANDA211075
Company
Context & Analysis
GRANULES has 21 FDA actions in our database.
Frequently Asked Questions
How often does GRANULES have FDA actions?
GRANULES has 21 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 "ANDA211075-8" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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