Lurasidone Hydrochloride 38217-0014
Product NDC
38217-0014- Manufacturer
- Sumitomo Pharma Co., Ltd.
- Dosage Form
- Tablet, Film Coated
- Product Type
- Drug For Further Processing
- Marketing Start
- May 21, 2014
- Listing Expires
- December 31, 2026
Active Ingredients
| Ingredient | Strength |
|---|---|
| Lurasidone Hydrochloride | 80 mg/1 |
Packaging Options(1)
50000 TABLET, FILM COATED in 1 DRUM (38217-0014-1)