FDA NDC Directory · JSON-LD · Markdown

Citalopram

NDC 50090-7419 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameCitalopram Hydrobromide
Labeler / ManufacturerA-S Medication Solutions
Marketing categoryAbbreviated NDA (generic) · App ANDA077031
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCITALOPRAM HYDROBROMIDE (10 mg/1)
Marketing started20041028
Package count3

External sources

Source: openFDA. Public-domain (CC0).