Active Ingredient: METHYLPHENIDATE HYDROCHLORIDE
Proprietary Name: METHYLPHENIDATE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 10MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A207488
Product Number: 001
Approval Date: Jun 9, 2015
Applicant Holder Full Name: ABHAI LLC
Marketing Status:
Prescription
Patent and Exclusivity Information
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: Yes
TE Code: AB
Application Number: A207488
Product Number: 002
Approval Date: Jun 9, 2015
Applicant Holder Full Name: ABHAI LLC
Marketing Status:
Prescription
Patent and Exclusivity Information