FDA Drug Application (076939) for PRAVASTATIN SODIUM by WATSON LABS

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Application Number076939
Product Number001
FormTABLET;ORAL
Dosage80MG
Product Market Status Prescription
Therapeutic Equivalence Evaluation Code AB Products meeting necessary bioequivalence requirements
Reference Drug
Drug NamePRAVASTATIN SODIUM
Active IngredientPRAVASTATIN SODIUM

Active IngredientCount
List of drugs with Active Ingredient PRAVASTATIN SODIUM3


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