Active Ingredient: DEXMETHYLPHENIDATE HYDROCHLORIDE
Proprietary Name: DEXMETHYLPHENIDATE HYDROCHLORIDE
Dosage Form; Route of Administration: CAPSULE, EXTENDED RELEASE; ORAL
Strength: 30MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A202580
Product Number: 001
Approval Date: Aug 28, 2013
Applicant Holder Full Name: AUROLIFE PHARMA LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information