FDA NDC Directory · JSON-LD · Markdown

Escitalopram

NDC 59746-281 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameEscitalopram Oxalate
Labeler / ManufacturerJubilant Cadista Pharmacuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA202280
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsESCITALOPRAM OXALATE (20 mg/1)
Marketing started20240101
Package count5

External sources

Source: openFDA. Public-domain (CC0).