Drugplain

NDC 43598-351-05

Lurasidone hydrochloride 20 mg/1

Lurasidone hydrochloride · TABLET, FILM COATED

No Recall History

Lurasidone hydrochloride is a tablet, film coated containing lurasidone hydrochloride at a strength of 20 mg/1. Manufactured by Dr. Reddys Laboratories Inc.

Key Facts

Brand Name
Lurasidone hydrochloride
Generic Name
Lurasidone hydrochloride
NDC Code (Package)
43598-351-05
NDC Code (Product)
43598-351
Manufacturer
Dr. Reddys Laboratories Inc
Strength
20 mg/1
Dosage Form
TABLET, FILM COATED
Route
ORAL
Marketing Status
Application #
ANDA208047
Marketing Start
02/20/2023

Recall History

No Recall History

Not medical advice. This information is for reference only. Always consult your doctor or pharmacist.