FDA NDC Directory · JSON-LD · Markdown

escitalopram

NDC 16571-756 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerRising Pharma Holdings, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078777
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsESCITALOPRAM OXALATE (10 mg/1)
Marketing started20230610
Package count2

External sources

Source: openFDA. Public-domain (CC0).