Strength
20 mg/1
Manufacturer
Lupin Pharmaceuticals Inc.NDC
68180067006
Classification
Generic
Dosage Form
TABLET
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
LURASIDONE HYDROCHLORIDEApproval Type
Generic (ANDA)
FDA Application
ANDA208031On Market Since
2/20/2023
Pharmacological Classes
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