Lurasidone Hydrochloride 47335-0639
Product NDC
47335-0639- 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
Need to source Lurasidone Hydrochloride? Find it on a pharmacy-to-pharmacy marketplace at better prices.
✓ DSCSA Compliant. ✓ Verified Pharmacies Only.P2P pharmacy marketplace.
Active Ingredients
| Ingredient | Strength |
|---|---|
| Lurasidone Hydrochloride | 60 mg/1 |
Drug Class
Atypical Antipsychotic [EPC]
Packaging Options(3)
500 TABLET in 1 BOTTLE (47335-639-13)
90 TABLET in 1 BOTTLE (47335-639-81)
30 TABLET in 1 BOTTLE (47335-639-83)