FDA NDC Directory · JSON-LD · Markdown

Clonidine

NDC 50742-247 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Generic nameclonidine
Labeler / ManufacturerIngenus Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA209675
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsCLONIDINE HYDROCHLORIDE (.1 mg/1)
Marketing started20190305
Package count3

External sources

Source: openFDA. Public-domain (CC0).