FDA Drug Application (202633) for PRAMIPEXOLE DIHYDROCHLORIDE by AUROBINDO PHARMA LTD

Back to FDA Applications sponsored by AUROBINDO PHARMA LTD

Application Number202633
Product Number001
FormTABLET;ORAL
Dosage0.125MG
Product Market Status Prescription
Therapeutic Equivalence Evaluation Code AB Products meeting necessary bioequivalence requirements
Reference Drug
Drug NamePRAMIPEXOLE DIHYDROCHLORIDE
Active IngredientPRAMIPEXOLE DIHYDROCHLORIDE

Active IngredientCount
List of drugs with Active Ingredient PRAMIPEXOLE DIHYDROCHLORIDE3


Back to FDA Applications sponsored by AUROBINDO PHARMA LTD