FDA NDC Directory · JSON-LD · Markdown

Clonidine hydrochloride

NDC 52817-182 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerTruPharma, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA070923
Dosage form / routeTABLET · ORAL
Active ingredientsCLONIDINE HYDROCHLORIDE (.3 mg/1)
Marketing started20170601
Package count3

External sources

Source: openFDA. Public-domain (CC0).