NDC 50228-430

Droxidopa 200 mg capsule

On the label: ScieGen Pharmaceuticals, Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
ScieGen Pharmaceuticals, INC.Hauppauge, NY, United StatesMakes it and tests it Problems found, fixed voluntarilyMay 15, 2026 · 15 inspections, 1 with FDA action

Product details

Generic drug
Droxidopa: every company that makes it
Form
capsule, oral
Strength
200 mg
Approval
ANDA ANDA214017
On the market since
Feb 18, 2021
Package NDCs
50228-430-10 50228-430-30 50228-430-90
Official label
DailyMed (National Library of Medicine), updated Feb 19, 2021

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