Active Ingredient: METHYLPHENIDATE HYDROCHLORIDE
Proprietary Name: METHYLPHENIDATE HYDROCHLORIDE
Dosage Form; Route of Administration: SOLUTION; ORAL
Strength: 5MG/5ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AA
Application Number: A207417
Product Number: 001
Approval Date: Jan 29, 2021
Applicant Holder Full Name: ASCENT PHARMACEUTICALS INC
Marketing Status:
Prescription
Patent and Exclusivity Information
Active Ingredient: METHYLPHENIDATE HYDROCHLORIDE
Proprietary Name: METHYLPHENIDATE HYDROCHLORIDE
Dosage Form; Route of Administration: SOLUTION; ORAL
Strength: 10MG/5ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AA
Application Number: A207417
Product Number: 002
Approval Date: Jan 29, 2021
Applicant Holder Full Name: ASCENT PHARMACEUTICALS INC
Marketing Status:
Prescription
Patent and Exclusivity Information