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Escitalopram Oxalate

NDC 33342-037 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerMacleods Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA202210
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsESCITALOPRAM OXALATE (10 mg/21)
Marketing started20120911
Package count3

External sources

Source: openFDA. Public-domain (CC0).