FdaApplication

NDA 019439

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Identifiers

Properties

PropertyValue
applicant_nameMERCK INC
application_typeNDA
approval_date1986-06-13

Products (2)

ProductActive ingredientStrengthDosage form
POTASSIUM CHLORIDEPOTASSIUM CHLORIDE10MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET, EXTENDED RELEASE;ORAL
POTASSIUM CHLORIDEPOTASSIUM CHLORIDE20MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET, EXTENDED RELEASE;ORAL

2 products