RISPERDAL CONSTA (RISPERIDONE)
Summary
FDA approved RISPERDAL CONSTA (RISPERIDONE) by JANSSEN PHARMS. NDA (New Drug) approval (Labeling) on 2025-01-22. POWDER, INTRAMUSCULAR.
Details
Source
Drug Approval
External ID
NDA021346-65
Action Date
2025-01-22
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
RISPERDAL CONSTA (generic: RISPERIDONE), POWDER, INTRAMUSCULAR. Application: NDA021346
Company
Context & Analysis
JANSSEN PHARMS has 10 FDA actions in our database.
Frequently Asked Questions
How often does JANSSEN PHARMS have FDA actions?
JANSSEN PHARMS has 10 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 "NDA021346-65" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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