FDA NDC Directory · JSON-LD · Markdown

Clonidine Hydrochloride

NDC 58657-649 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerMethod Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA202297
Dosage form / routeTABLET · ORAL
Active ingredientsCLONIDINE HYDROCHLORIDE (.3 mg/1)
Marketing started20200701
Package count3

External sources

Source: openFDA. Public-domain (CC0).