Lurasidone Hydrochloride 31722-0081-90

Package NDC

31722-0081-90

Manufacturer: Camber Pharmaceuticals, Inc.
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: August 21, 2024
Listing Expires: December 31, 2026
Application: ANDA218174

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Active Ingredients

Ingredient	Strength
Lurasidone Hydrochloride	40 mg/1

Drug Class

Atypical Antipsychotic [EPC]

Selected Package

31722-0081-90Selected

90 TABLET, FILM COATED in 1 BOTTLE (31722-081-90)

Other packages for this product(2)

31722-0081-05

500 TABLET, FILM COATED in 1 BOTTLE (31722-081-05)

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31722-0081-30

30 TABLET, FILM COATED in 1 BOTTLE (31722-081-30)

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