Lurasidone Hydrochloride 23155-0888
Product NDC
23155-0888- Manufacturer
- Heritage Pharma Labs Inc. D/b/a Avet Pharmaceuticals Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 19, 2023
- Listing Expires
- December 31, 2026
- Application
- ANDA208058
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Lurasidone Hydrochloride | 40 mg/1 |
Drug Class
Atypical Antipsychotic [EPC]
Packaging Options(4)
30 TABLET, FILM COATED in 1 BOTTLE (23155-888-03)
500 TABLET, FILM COATED in 1 BOTTLE (23155-888-05)
90 TABLET, FILM COATED in 1 BOTTLE (23155-888-09)
60500 TABLET, FILM COATED in 1 CONTAINER (23155-888-18)