FDA Drug Application (062378) for ULTRACEF by BRISTOL

Back to FDA Applications sponsored by BRISTOL

Application Number062378
Product Number001
FormCAPSULE;ORAL
DosageEQ 500MG BASE
Product Market Status Discontinued
Therapeutic Equivalence Evaluation Code
Reference Drug
Drug NameULTRACEF
Active IngredientCEFADROXIL/CEFADROXIL HEMIHYDRATE

Active IngredientCount
List of drugs with Active Ingredient CEFADROXIL/CEFADROXIL HEMIHYDRATE3


Back to FDA Applications sponsored by BRISTOL