FDA NDC Directory · JSON-LD · Markdown

droxidopa

NDC 63304-112 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA214384
Dosage form / routeCAPSULE · ORAL
Active ingredientsDROXIDOPA (300 ug/1)
Marketing started20210218
Package count1

External sources

Source: openFDA. Public-domain (CC0).