FDA NDC Directory · JSON-LD · Markdown

Clonidine hydrochloride

NDC 60687-462 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA209686
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsCLONIDINE HYDROCHLORIDE (.1 mg/1)
Marketing started20191217
Package count1

External sources

Source: openFDA. Public-domain (CC0).