LOXITANE C
Summary
FDA approved LOXITANE C by TEVA BRANDED PHARM. NDA (New Drug) approval (Labeling) on 2025-01-22. CONCENTRATE, ORAL.
Details
Source
Drug Approval
External ID
NDA017658-39
Action Date
2025-01-22
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
LOXITANE C, CONCENTRATE, ORAL. Application: NDA017658
Company
Context & Analysis
TEVA BRANDED PHARM has 8 FDA actions in our database.
Frequently Asked Questions
How often does TEVA BRANDED PHARM have FDA actions?
TEVA BRANDED PHARM has 8 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 "NDA017658-39" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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