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Eletriptan Hydrobromide

NDC 63629-8320 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA210708
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsELETRIPTAN HYDROBROMIDE (40 mg/1)
Marketing started20180216
Package count2

External sources

Source: openFDA. Public-domain (CC0).