FdaApplication

ANDA 071536

Back to search

Identifiers

Properties

PropertyValue
applicant_nameSUN PHARMACEUTICAL INDUSTRIES INC
application_typeANDA
approval_date1993-04-28

Products (2)

ProductActive ingredientStrengthDosage form
METOCLOPRAMIDE HYDROCHLORIDEMETOCLOPRAMIDE HYDROCHLORIDEEQ 10MG BASETABLET;ORAL
METOCLOPRAMIDE HYDROCHLORIDEMETOCLOPRAMIDE HYDROCHLORIDEEQ 5MG BASETABLET;ORAL

2 products