FDA NDC Directory · JSON-LD · Markdown

Droxidopa

NDC 59651-375 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA214387
Dosage form / routeCAPSULE · ORAL
Active ingredientsDROXIDOPA (100 mg/1)
Marketing started20210218
Package count1

External sources

Source: openFDA. Public-domain (CC0).