Lurasidone Hydrochloride 72603-0622
Product NDC
72603-0622- Manufacturer
- Northstar Rxllc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- April 8, 2025
- Listing Expires
- December 31, 2026
- Application
- ANDA212124
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Lurasidone Hydrochloride | 40 mg/1 |
Drug Class
Atypical Antipsychotic [EPC]
Packaging Options(1)
30 TABLET, FILM COATED in 1 BOTTLE (72603-622-01)