Lurasidone Hydrochloride 67046-1637
Product NDC
67046-1637- Manufacturer
- Coupler Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- December 31, 2025
- Listing Expires
- December 31, 2026
- Application
- ANDA213248
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Lurasidone Hydrochloride | 40 mg/1 |
Drug Class
Atypical Antipsychotic [EPC]
Packaging Options(1)
30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1637-3)