ALLERGY RELIEF (CETIRIZINE HYDROCHLORIDE)
Summary
FDA approved ALLERGY RELIEF (CETIRIZINE HYDROCHLORIDE) by MARKSANS PHARMA. ANDA (Generic) approval (Manufacturing (CMC)) on 2023-04-13. TABLET, ORAL.
Details
Source
Drug Approval
External ID
ANDA078933-5
Action Date
2023-04-13
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
ALLERGY RELIEF (generic: CETIRIZINE HYDROCHLORIDE), TABLET, ORAL. Application: ANDA078933
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 "ANDA078933-5" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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