FDA NDC Directory · JSON-LD · Markdown

Dexmedetomidine Hydrochloride

NDC 68083-239 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerGland Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA209307
Dosage form / routeINJECTION · INTRAVENOUS
Active ingredientsDEXMEDETOMIDINE HYDROCHLORIDE (4 ug/mL)
Marketing started20200603
Package count1

External sources

Source: openFDA. Public-domain (CC0).