FDA NDC Directory · JSON-LD · Markdown

Clonidine Hydrochloride

NDC 70518-4342 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA070974
Dosage form / routeTABLET · ORAL
Active ingredientsCLONIDINE HYDROCHLORIDE (.1 mg/1)
Marketing started20250518
Package count2

External sources

Source: openFDA. Public-domain (CC0).