TENORMIN (ATENOLOL)
Summary
FDA approved TENORMIN (ATENOLOL) by TWI PHARMS. NDA (New Drug) approval (Labeling) on 2023-12-22. TABLET, ORAL.
Details
Source
Drug Approval
External ID
NDA018240-47
Action Date
2023-12-22
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
TENORMIN (generic: ATENOLOL), TABLET, ORAL. Application: NDA018240
Company
Context & Analysis
TWI PHARMS has 9 FDA actions in our database.
Frequently Asked Questions
How often does TWI PHARMS have FDA actions?
TWI PHARMS has 9 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 "NDA018240-47" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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