FdaApplication

ANDA 219557

Back to search

Identifiers

Properties

PropertyValue
applicant_nameGLENMARK PHARMACEUTICALS INC USA
application_typeANDA
approval_date2025-02-28

Products (1)

ProductActive ingredientStrengthDosage form
OLOPATADINE HYDROCHLORIDEOLOPATADINE HYDROCHLORIDEEQ 0.2% BASESOLUTION/DROPS;OPHTHALMIC

1 product