LORATADINE 10 MG (LORATADINE TABLETS USP, 10 MG)
Summary
FDA approved LORATADINE 10 MG (LORATADINE TABLETS USP, 10 MG) by MARKSANS PHARMA. ANDA (Generic) approval on 2024-11-21. TABLET, ORAL.
Details
Source
Drug Approval
External ID
ANDA219223-1
Action Date
2024-11-21
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
LORATADINE 10 MG (generic: LORATADINE TABLETS USP, 10 MG), TABLET, ORAL. Application: ANDA219223
Company
Context & Analysis
MARKSANS PHARMA has 8 FDA actions in our database.
Frequently Asked Questions
How often does MARKSANS PHARMA have FDA actions?
MARKSANS PHARMA has 8 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 "ANDA219223-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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