NEVIRAPINE
Summary
FDA approved NEVIRAPINE by MYLAN. ANDA (Generic) approval (Labeling) on 2024-08-22. TABLET, EXTENDED RELEASE, ORAL.
Details
Source
Drug Approval
External ID
ANDA205651-7
Action Date
2024-08-22
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
NEVIRAPINE, TABLET, EXTENDED RELEASE, ORAL. Application: ANDA205651
Company
Context & Analysis
MYLAN has 44 FDA actions in our database.
Frequently Asked Questions
How often does MYLAN have FDA actions?
MYLAN has 44 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 "ANDA205651-7" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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