METHYLPHENIDATE HYDROCHLORIDE
Summary
FDA approved METHYLPHENIDATE HYDROCHLORIDE by AMNEAL PHARMS. ANDA (Generic) approval (Labeling) on 2024-05-15. TABLET, EXTENDED RELEASE, ORAL.
Details
Source
Drug Approval
External ID
ANDA207515-17
Action Date
2024-05-15
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
METHYLPHENIDATE HYDROCHLORIDE, TABLET, EXTENDED RELEASE, ORAL. Application: ANDA207515
Company
Context & Analysis
AMNEAL PHARMS has 43 FDA actions in our database.
Frequently Asked Questions
How often does AMNEAL PHARMS have FDA actions?
AMNEAL PHARMS has 43 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 "ANDA207515-17" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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