FDA NDC Directory · JSON-LD · Markdown

Escitalopram

NDC 51655-147 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameEscitalopram Oxalate
Labeler / ManufacturerNorthwind Health Company, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA090432
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsESCITALOPRAM OXALATE (20 mg/1)
Marketing started20230125
Package count1

External sources

Source: openFDA. Public-domain (CC0).