Active Ingredient: DEXMETHYLPHENIDATE HYDROCHLORIDE
Proprietary Name: DEXMETHYLPHENIDATE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 10MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A209211
Product Number: 002
Approval Date: Sep 19, 2018
Applicant Holder Full Name: CEDIPROF INC
Marketing Status:
Prescription
Patent and Exclusivity Information