Active Ingredient: METHYLPHENIDATE HYDROCHLORIDE
Proprietary Name: METHYLPHENIDATE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 20MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A212288
Product Number: 001
Approval Date: Oct 6, 2020
Applicant Holder Full Name: ALKEM LABORATORIES LTD
Marketing Status:
Prescription
Patent and Exclusivity Information