Lurasidone Hydrochloride 60687-0747
Product NDC
60687-0747- Manufacturer
- American Health Packaging
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 5, 2023
- Listing Expires
- December 31, 2026
- Application
- ANDA212244
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Lurasidone Hydrochloride | 20 mg/1 |
Drug Class
Atypical Antipsychotic [EPC]
Packaging Options(1)
30 BLISTER PACK in 1 CARTON (60687-747-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-747-11)