FDA NDC Directory · JSON-LD · Markdown

escitalopram

NDC 68788-8569 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerPreferred Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078777
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsESCITALOPRAM OXALATE (10 mg/1)
Marketing started20240123
Package count4

External sources

Source: openFDA. Public-domain (CC0).