NDC 69367-340

Carbidopa and Levodopa 25 mg / 250 mg tablet

On the label: Westminster Pharmaceuticals, LLC.

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
ScieGen Pharmaceuticals, INC.Hauppauge, NY, United StatesMakes it, tests it, packages it and labels 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
Sep 30, 2021
Package NDCs
69367-340-01 69367-340-05
Official label
DailyMed (National Library of Medicine), updated May 27, 2026

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