FDA NDC Directory · JSON-LD · Markdown

Clonidine hydrochloride

NDC 71205-588 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA070925
Dosage form / routeTABLET · ORAL
Active ingredientsCLONIDINE HYDROCHLORIDE (.1 mg/1)
Marketing started20170601
Package count4

External sources

Source: openFDA. Public-domain (CC0).