Lurasidone Hydrochloride 72205-0210
Product NDC
72205-0210- Manufacturer
- Novadoz Pharmaceuticals Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- February 9, 2023
- Listing Expires
- December 31, 2026
- Application
- ANDA208037
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Lurasidone Hydrochloride | 80 mg/1 |
Drug Class
Atypical Antipsychotic [EPC]
Packaging Options(3)
500 TABLET, FILM COATED in 1 BOTTLE (72205-210-05)
30 TABLET, FILM COATED in 1 BOTTLE (72205-210-30)
90 TABLET, FILM COATED in 1 BOTTLE (72205-210-90)