FDA Drug Application (070652) for METHYLDOPATE HYDROCHLORIDE by ABRAXIS PHARM

Back to FDA Applications sponsored by ABRAXIS PHARM

Application Number070652
Product Number001
FormINJECTABLE;INJECTION
Dosage50MG/ML
Product Market Status Discontinued
Therapeutic Equivalence Evaluation Code
Reference Drug
Drug NameMETHYLDOPATE HYDROCHLORIDE
Active IngredientMETHYLDOPATE HYDROCHLORIDE

Active IngredientCount
List of drugs with Active Ingredient METHYLDOPATE HYDROCHLORIDE3


Back to FDA Applications sponsored by ABRAXIS PHARM