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clonidine hydrochloride

NDC 46708-307 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameClonidine Hydrochloride
Labeler / ManufacturerAlembic Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA091368
Dosage form / routeTABLET · ORAL
Active ingredientsCLONIDINE HYDROCHLORIDE (.2 mg/1)
Marketing started20160503
Package count5

External sources

Source: openFDA. Public-domain (CC0).