PAROXETINE HYDROCHLORIDE
Summary
FDA approved PAROXETINE HYDROCHLORIDE by PRINSTON INC. ANDA (Generic) approval on 2024-01-04. TABLET, EXTENDED RELEASE, ORAL.
Details
Source
Drug Approval
External ID
ANDA209748-1
Action Date
2024-01-04
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
PAROXETINE HYDROCHLORIDE, TABLET, EXTENDED RELEASE, ORAL. Application: ANDA209748
Company
Context & Analysis
PRINSTON INC has 25 FDA actions in our database.
Frequently Asked Questions
How often does PRINSTON INC have FDA actions?
PRINSTON INC has 25 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 "ANDA209748-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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