LEVOTHYROXINE SODIUM
Summary
FDA approved LEVOTHYROXINE SODIUM by WATSON LABS TEVA. ANDA (Generic) approval (Labeling) on 2024-09-10. TABLET, ORAL.
Details
Source
Drug Approval
External ID
ANDA207588-6
Action Date
2024-09-10
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
LEVOTHYROXINE SODIUM, TABLET, ORAL. Application: ANDA207588
Company
Context & Analysis
WATSON LABS TEVA has 5 FDA actions in our database.
Frequently Asked Questions
How often does WATSON LABS TEVA have FDA actions?
WATSON LABS TEVA has 5 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 "ANDA207588-6" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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