FDA Drug Application (078551) for PRAMIPEXOLE DIHYDROCHLORIDE by WATSON LABS

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Application Number078551
Product Number001
FormTABLET;ORAL
Dosage0.125MG
Product Market Status Discontinued
Therapeutic Equivalence Evaluation Code
Reference Drug
Drug NamePRAMIPEXOLE DIHYDROCHLORIDE
Active IngredientPRAMIPEXOLE DIHYDROCHLORIDE

Active IngredientCount
List of drugs with Active Ingredient PRAMIPEXOLE DIHYDROCHLORIDE3


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