FDA NDC Directory · JSON-LD · Markdown

Escitalopram

NDC 68071-4985 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerNuCare Pharmaceuticals,Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA202389
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsESCITALOPRAM OXALATE (20 mg/1)
Marketing started20130321
Package count1

External sources

Source: openFDA. Public-domain (CC0).