FDA Drug Application (062127) for UTIMOX by PARKE DAVIS

Back to FDA Applications sponsored by PARKE DAVIS

Application Number062127
Product Number001
FormFOR SUSPENSION;ORAL
Dosage125MG/5ML
Product Market Status Discontinued
Therapeutic Equivalence Evaluation Code
Reference Drug
Drug NameUTIMOX
Active IngredientAMOXICILLIN

Active IngredientCount
List of drugs with Active Ingredient AMOXICILLIN22


Back to FDA Applications sponsored by PARKE DAVIS