Lurasidone Hydrochloride 67877-0640
Product NDC
67877-0640- Manufacturer
- Ascend Laboratories, Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 4, 2023
- Listing Expires
- December 31, 2026
- Application
- ANDA212244
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Lurasidone Hydrochloride | 60 mg/1 |
Drug Class
Atypical Antipsychotic [EPC]
Packaging Options(4)
500 TABLET, FILM COATED in 1 BOTTLE (67877-640-05)
30 TABLET, FILM COATED in 1 BOTTLE (67877-640-30)
10 BLISTER PACK in 1 CARTON (67877-640-38) / 10 TABLET, FILM COATED in 1 BLISTER PACK (67877-640-33)
90 TABLET, FILM COATED in 1 BOTTLE (67877-640-90)