Lurasidone Hydrochloride 43598-0354
Product NDC
43598-0354- Manufacturer
- Dr. Reddys Laboratories Inc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- February 20, 2023
- Listing Expires
- December 31, 2026
- Application
- ANDA208047
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Lurasidone Hydrochloride | 80 mg/1 |
Drug Class
Atypical Antipsychotic [EPC]
Packaging Options(4)
500 TABLET, FILM COATED in 1 BOTTLE (43598-354-05)
30 TABLET, FILM COATED in 1 BOTTLE (43598-354-30)
10 BLISTER PACK in 1 CARTON (43598-354-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (43598-354-79)
90 TABLET, FILM COATED in 1 BOTTLE (43598-354-90)