PAROXETINE HYDROCHLORIDE
Summary
FDA approved PAROXETINE HYDROCHLORIDE by EPIC PHARMA LLC. ANDA (Generic) approval (Manufacturing (CMC)) on 2022-05-26. TABLET, EXTENDED RELEASE, ORAL.
Details
Source
Drug Approval
External ID
ANDA213612-1
Action Date
2022-05-26
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
PAROXETINE HYDROCHLORIDE, TABLET, EXTENDED RELEASE, ORAL. Application: ANDA213612
Company
Context & Analysis
EPIC PHARMA LLC has 27 FDA actions in our database.
Frequently Asked Questions
How often does EPIC PHARMA LLC have FDA actions?
EPIC PHARMA LLC has 27 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 "ANDA213612-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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