FdaApplication

ANDA 090918

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Identifiers

Properties

PropertyValue
applicant_nameAPOTEX INC
application_typeANDA
approval_date2017-12-05

Products (1)

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

1 product