FDA NDC Directory · JSON-LD · Markdown

clonidine hydrochloride

NDC 50268-192 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAvPAK
Marketing categoryAbbreviated NDA (generic) · App ANDA078895
Dosage form / routeTABLET · ORAL
Active ingredientsCLONIDINE HYDROCHLORIDE (.1 mg/1)
Marketing started20230530
Package count1

External sources

Source: openFDA. Public-domain (CC0).