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Cyproheptadine Hydrochloride

NDC 0115-1757 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAmneal Pharmaceuticals of New York LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA040537
Dosage form / routeTABLET · ORAL
Active ingredientsCYPROHEPTADINE HYDROCHLORIDE (4 mg/1)
Marketing started20150729
Package count2

External sources

Source: openFDA. Public-domain (CC0).