FDA NDC Directory · JSON-LD · Markdown

Citalopram

NDC 51655-137 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerNorthwind Health Company, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA077534
Dosage form / routeTABLET · ORAL
Active ingredientsCITALOPRAM HYDROBROMIDE (20 mg/1)
Marketing started20221004
Package count2

External sources

Source: openFDA. Public-domain (CC0).