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Escitalopram

NDC 0615-8476 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameEscitalopram Oxalate
Labeler / ManufacturerNCS HealthCare of KY, LLC dba Vangard Labs
Marketing categoryAbbreviated NDA (generic) · App ANDA090432
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsESCITALOPRAM OXALATE (10 mg/1)
Marketing started20120911
Package count3

External sources

Source: openFDA. Public-domain (CC0).