FdaApplication

NDA 011635

Back to search

Identifiers

Properties

PropertyValue
applicant_nameMERCK AND CO INC
application_typeNDA
approval_date1987-08-26

Products (2)

ProductActive ingredientStrengthDosage form
DIUPRES-250CHLOROTHIAZIDE; RESERPINE250MG;0.125MGTABLET;ORAL
DIUPRES-500CHLOROTHIAZIDE; RESERPINE500MG;0.125MGTABLET;ORAL

2 products