TERAZOSIN
Summary
FDA approved TERAZOSIN by BIONPHARMA. ANDA (Generic) approval (Manufacturing (CMC)) on 2024-01-19. CAPSULE, ORAL.
Details
Source
Drug Approval
External ID
ANDA075667-2
Action Date
2024-01-19
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
TERAZOSIN, CAPSULE, ORAL. Application: ANDA075667
Company
Context & Analysis
BIONPHARMA has 27 FDA actions in our database.
Frequently Asked Questions
How often does BIONPHARMA have FDA actions?
BIONPHARMA 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 "ANDA075667-2" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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