FdaApplication

ANDA 065081

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Identifiers

Properties

PropertyValue
applicant_nameSUN PHARMACEUTICAL INDUSTRIES LTD
application_typeANDA
approval_date2001-07-27

Products (2)

ProductActive ingredientStrengthDosage form
CEPHALEXINCEPHALEXINEQ 250MG BASE/5MLFOR SUSPENSION;ORAL
CEPHALEXINCEPHALEXINEQ 125MG BASE/5MLFOR SUSPENSION;ORAL

2 products