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Citalopram

NDC 42708-019 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameCitalopram Hydrobromide
Labeler / ManufacturerQPharma, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA077031
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCITALOPRAM HYDROBROMIDE (20 mg/1)
Marketing started20041028
Package count1

External sources

Source: openFDA. Public-domain (CC0).