FDA NDC Directory · JSON-LD · Markdown

CYPROHEPTADINE HYDROCHLORIDE

NDC 70752-232 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerQuagen Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA212491
Dosage form / routeTABLET · ORAL
Active ingredientsCYPROHEPTADINE HYDROCHLORIDE (2 mg/1)
Marketing started20261015
Package count2

External sources

Source: openFDA. Public-domain (CC0).