Active Ingredient: RAMELTEON
Proprietary Name: RAMELTEON
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 8MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A211567
Product Number: 001
Approval Date: Jul 22, 2019
Applicant Holder Full Name: ZYDUS PHARMACEUTICALS USA INC
Marketing Status:
Prescription
Patent and Exclusivity Information