FDA NDC Directory · JSON-LD · Markdown

CYPROHEPTADINE HYDROCHLORIDE

NDC 50742-190 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerIngenus Pharmaceuticals LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA205087
Dosage form / routeTABLET · ORAL
Active ingredientsCYPROHEPTADINE HYDROCHLORIDE (4 mg/1)
Marketing started20150923
Package count2

External sources

Source: openFDA. Public-domain (CC0).