FDA NDC Directory · JSON-LD · Markdown

Droxidopa

NDC 72205-072 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerNovadoz Pharmaceuticals LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA211741
Dosage form / routeCAPSULE · ORAL
Active ingredientsDROXIDOPA (100 mg/1)
Marketing started20210219
Package count2

External sources

Source: openFDA. Public-domain (CC0).