FDA Drug Application (087999) for SPIRONOLACTONE AND HYDROCHLOROTHIAZIDE by PUREPAC PHARM

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Application Number087999
Product Number001
FormTABLET;ORAL
Dosage25MG;25MG
Product Market Status Discontinued
Therapeutic Equivalence Evaluation Code
Reference Drug
Drug NameSPIRONOLACTONE AND HYDROCHLOROTHIAZIDE
Active IngredientHYDROCHLOROTHIAZIDE; SPIRONOLACTONE

Active IngredientCount
List of drugs with Active Ingredient HYDROCHLOROTHIAZIDE122
List of drugs with Active Ingredient SPIRONOLACTONE5


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