Strength
80 mg/1
Manufacturer
Sun Pharmaceutical Industries Inc.NDC
47335068583
Classification
Generic
Dosage Form
TABLET
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
LURASIDONE HYDROCHLORIDEApproval Type
Generic (ANDA)
FDA Application
ANDA208066On Market Since
2/20/2023
Pharmacological Classes
LURASIDONE HCL 80 MG TABLET
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