Active Ingredient: PRAMIPEXOLE DIHYDROCHLORIDE
Proprietary Name: PRAMIPEXOLE DIHYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 0.75MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A090764
Product Number: 001
Approval Date: Apr 9, 2010
Applicant Holder Full Name: MYLAN PHARMACEUTICALS INC
Marketing Status:
Discontinued
Patent and Exclusivity Information