FDA NDC Directory · JSON-LD · Markdown

clonidine hydrochloride

NDC 68788-8494 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerPreferred Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078895
Dosage form / routeTABLET · ORAL
Active ingredientsCLONIDINE HYDROCHLORIDE (.1 mg/1)
Marketing started20230726
Package count4

External sources

Source: openFDA. Public-domain (CC0).