Lurasidone Hydrochloride 68382-0965
Product NDC
68382-0965- Manufacturer
- Zydus Pharmaceuticals Usa Inc.
- 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 | 20 mg/1 |
Drug Class
Atypical Antipsychotic [EPC]
Packaging Options(5)
100 TABLET, COATED in 1 BOTTLE (68382-965-01)
500 TABLET, COATED in 1 BOTTLE (68382-965-05)
30 TABLET, COATED in 1 BOTTLE (68382-965-06)
90 TABLET, COATED in 1 BOTTLE (68382-965-16)
100 BLISTER PACK in 1 CARTON (68382-965-77) / 1 TABLET, COATED in 1 BLISTER PACK (68382-965-30)