Lurasidone Hydrochloride 67877-0641
Product NDC
67877-0641- 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
Need to source Lurasidone Hydrochloride? Find it on a pharmacy-to-pharmacy marketplace at better prices.
✓ DSCSA Compliant. ✓ Verified Pharmacies Only.P2P pharmacy marketplace.
Active Ingredients
| Ingredient | Strength |
|---|---|
| Lurasidone Hydrochloride | 80 mg/1 |
Drug Class
Atypical Antipsychotic [EPC]
Packaging Options(4)
500 TABLET, FILM COATED in 1 BOTTLE (67877-641-05)
30 TABLET, FILM COATED in 1 BOTTLE (67877-641-30)
10 BLISTER PACK in 1 CARTON (67877-641-38) / 10 TABLET, FILM COATED in 1 BLISTER PACK (67877-641-33)
90 TABLET, FILM COATED in 1 BOTTLE (67877-641-90)