FDA Drug Application (020729) for UNIRETIC by UCB INC

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Application Number020729
Product Number001
FormTABLET;ORAL
Dosage12.5MG;7.5MG
Product Market Status Discontinued
Therapeutic Equivalence Evaluation Code
Reference Drug
Drug NameUNIRETIC
Active IngredientHYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE

Active IngredientCount
List of drugs with Active Ingredient HYDROCHLOROTHIAZIDE122
List of drugs with Active Ingredient MOEXIPRIL HYDROCHLORIDE5


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