FDA Drug Application (071819) for METHYLDOPA AND HYDROCHLOROTHIAZIDE by TEVA

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Application Number071819
Product Number001
FormTABLET;ORAL
Dosage15MG;250MG
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


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