FDA Drug Application (070544) for METHYLDOPA AND HYDROCHLOROTHIAZIDE by SANDOZ

Back to FDA Applications sponsored by SANDOZ

Application Number070544
Product Number001
FormTABLET;ORAL
Dosage50MG;500MG
Product Market Status Discontinued
Therapeutic Equivalence Evaluation Code
Reference Drug
Drug NameMETHYLDOPA AND HYDROCHLOROTHIAZIDE
Active IngredientHYDROCHLOROTHIAZIDE; METHYLDOPA

Active IngredientCount
List of drugs with Active Ingredient HYDROCHLOROTHIAZIDE122
List of drugs with Active Ingredient METHYLDOPA10


Back to FDA Applications sponsored by SANDOZ