Lurasidone Hydrochloride 70771-1737
Product NDC
70771-1737- Manufacturer
- Zydus Lifesciences Limited
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- February 1, 2023
- Listing Expires
- December 31, 2026
- Application
- ANDA208052
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Lurasidone Hydrochloride | 80 mg/1 |
Drug Class
Atypical Antipsychotic [EPC]
Packaging Options(5)
100 TABLET, COATED in 1 BOTTLE (70771-1737-1)
30 TABLET, COATED in 1 BOTTLE (70771-1737-3)
10 BLISTER PACK in 1 CARTON (70771-1737-4) / 10 TABLET, COATED in 1 BLISTER PACK (70771-1737-2)
500 TABLET, COATED in 1 BOTTLE (70771-1737-5)
90 TABLET, COATED in 1 BOTTLE (70771-1737-9)