NDC 50228-459

Carbidopa and Levodopa 25 mg / 250 mg tablet

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
Carbidopa and Levodopa: every company that makes it
Form
tablet, oral
Strength
25 mg / 250 mg
Approval
ANDA ANDA214092
On the market since
May 7, 2021
Package NDCs
50228-459-01 50228-459-05 50228-459-10 50228-459-30
Official label
DailyMed (National Library of Medicine), updated Apr 27, 2026

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