FDA Drug Application (200821) for PANTOPRAZOLE SODIUM by MACLEODS PHARMS LTD

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Application Number200821
Product Number001
FormTABLET, DELAYED RELEASE;ORAL
DosageEQ 20MG BASE
Product Market Status Prescription
Therapeutic Equivalence Evaluation Code AB Products meeting necessary bioequivalence requirements
Reference Drug
Drug NamePANTOPRAZOLE SODIUM
Active IngredientPANTOPRAZOLE SODIUM



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