Active Ingredient: ESZOPICLONE
Proprietary Name: ESZOPICLONE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 1MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A091103
Product Number: 001
Approval Date: Apr 3, 2013
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status:
Prescription
Patent and Exclusivity Information