EZALLOR SPRINKLE
Summary
FDA approved EZALLOR SPRINKLE by SUN PHARM. NDA (New Drug) approval (Labeling) on 2025-02-12. CAPSULE, ORAL.
Details
Source
Drug Approval
External ID
NDA208647-15
Action Date
2025-02-12
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
EZALLOR SPRINKLE, CAPSULE, ORAL. Application: NDA208647
Company
Context & Analysis
SUN PHARM has 48 FDA actions in our database.
Frequently Asked Questions
How often does SUN PHARM have FDA actions?
SUN PHARM has 48 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 "NDA208647-15" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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