FDA NDC Directory · JSON-LD · Markdown

clonidine hydrochloride

NDC 68788-8080 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameClonidine Hydrochloride
Labeler / ManufacturerPreferred Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA091368
Dosage form / routeTABLET · ORAL
Active ingredientsCLONIDINE HYDROCHLORIDE (.2 mg/1)
Marketing started20211005
Package count3

External sources

Source: openFDA. Public-domain (CC0).