FDA Drug Application (020987) for PROTONIX by WYETH PHARMS INC

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Application Number020987
Product Number001
FormTABLET, DELAYED RELEASE;ORAL
DosageEQ 40MG BASE
Product Market Status Prescription
Therapeutic Equivalence Evaluation Code AB Products meeting necessary bioequivalence requirements
Reference Drug
Drug NamePROTONIX
Active IngredientPANTOPRAZOLE SODIUM

Active IngredientCount
List of drugs with Active Ingredient PANTOPRAZOLE SODIUM3


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