FDA NDC Directory · JSON-LD · Markdown

Citalopram

NDC 72162-2517 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameCitalopram Hydrobromide
Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA077031
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCITALOPRAM HYDROBROMIDE (20 mg/1)
Marketing started20041028
Package count2

External sources

Source: openFDA. Public-domain (CC0).