Lurasidone Hydrochloride 47335-0639-13
- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- February 20, 2023
- Listing Expires
- December 31, 2027
- Application
- ANDA208066
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Lurasidone Hydrochloride | 60 mg/1 |
Drug Class
Atypical Antipsychotic [EPC]
Selected Package
47335-0639-13Selected500 TABLET in 1 BOTTLE (47335-639-13)
Other packages for this product(2)
90 TABLET in 1 BOTTLE (47335-639-81)
30 TABLET in 1 BOTTLE (47335-639-83)