FDA NDC Directory · JSON-LD · Markdown

Citalopram Hydrobromide

NDC 51655-043 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerNorthwind Health Company, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA078216
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCITALOPRAM HYDROBROMIDE (10 mg/1)
Marketing started20210324
Package count2

External sources

Source: openFDA. Public-domain (CC0).