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Escitalopram Oxalate

NDC 69097-848 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameEscitalopram
Labeler / ManufacturerCipla USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078604
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsESCITALOPRAM OXALATE (10 mg/1)
Marketing started20160616
Package count5

External sources

Source: openFDA. Public-domain (CC0).