FDA NDC Directory · JSON-LD · Markdown

CYPROHEPTADINE HYDROCHLORIDE

NDC 70710-1110 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerZydus Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA208938
Dosage form / routeTABLET · ORAL
Active ingredientsCYPROHEPTADINE HYDROCHLORIDE (4 mg/1)
Marketing started20170720
Package count2

External sources

Source: openFDA. Public-domain (CC0).