MEMANTINE AND DONEPEZIL HYDROCHLORIDES
Summary
FDA approved MEMANTINE AND DONEPEZIL HYDROCHLORIDES by ANI PHARMS. ANDA (Generic) approval on 2023-12-15. CAPSULE, EXTENDED RELEASE, ORAL.
Details
Source
Drug Approval
External ID
ANDA208237-1
Action Date
2023-12-15
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
MEMANTINE AND DONEPEZIL HYDROCHLORIDES, CAPSULE, EXTENDED RELEASE, ORAL. Application: ANDA208237
Company
Context & Analysis
ANI PHARMS has 27 FDA actions in our database.
Frequently Asked Questions
How often does ANI PHARMS have FDA actions?
ANI PHARMS has 27 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 "ANDA208237-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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