U.S. flag An official website of the United States government

U.S. Food and Drug Administration
  1. Home
  2. Drug Databases
  3. Orange Book Home

Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

Home | Back to Search Results

Product Details for ANDA 208047

Expand all

LURASIDONE HYDROCHLORIDE (LURASIDONE HYDROCHLORIDE)
20MG
Marketing Status: Prescription
Active Ingredient: LURASIDONE HYDROCHLORIDE
Proprietary Name: LURASIDONE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 20MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A208047
Product Number: 001
Approval Date: Aug 24, 2021
Applicant Holder Full Name: DR REDDYS LABORATORIES LTD
Marketing Status:  Prescription
Patent and Exclusivity Information
LURASIDONE HYDROCHLORIDE (LURASIDONE HYDROCHLORIDE)
40MG
Marketing Status: Prescription
Active Ingredient: LURASIDONE HYDROCHLORIDE
Proprietary Name: LURASIDONE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 40MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A208047
Product Number: 002
Approval Date: Aug 24, 2021
Applicant Holder Full Name: DR REDDYS LABORATORIES LTD
Marketing Status:  Prescription
Patent and Exclusivity Information
LURASIDONE HYDROCHLORIDE (LURASIDONE HYDROCHLORIDE)
60MG
Marketing Status: Prescription
Active Ingredient: LURASIDONE HYDROCHLORIDE
Proprietary Name: LURASIDONE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 60MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A208047
Product Number: 003
Approval Date: Aug 24, 2021
Applicant Holder Full Name: DR REDDYS LABORATORIES LTD
Marketing Status:  Prescription
Patent and Exclusivity Information
LURASIDONE HYDROCHLORIDE (LURASIDONE HYDROCHLORIDE)
80MG
Marketing Status: Prescription
Active Ingredient: LURASIDONE HYDROCHLORIDE
Proprietary Name: LURASIDONE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 80MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A208047
Product Number: 004
Approval Date: Aug 24, 2021
Applicant Holder Full Name: DR REDDYS LABORATORIES LTD
Marketing Status:  Prescription
Patent and Exclusivity Information
Back to Top