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Eletriptan Hydrobromide

NDC 0378-4288 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameeletriptan hydrobromide
Labeler / ManufacturerMylan Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA205152
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsELETRIPTAN HYDROBROMIDE (40 mg/1)
Marketing started20170815
Package count2

External sources

Source: openFDA. Public-domain (CC0).