TEMOZOLOMIDE
Summary
FDA approved TEMOZOLOMIDE by SUN PHARM. ANDA (Generic) approval (Labeling) on 2026-01-22. CAPSULE, ORAL.
Details
Source
Drug Approval
External ID
ANDA201742-20
Action Date
2026-01-22
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
TEMOZOLOMIDE, CAPSULE, ORAL. Application: ANDA201742
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 "ANDA201742-20" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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