All FDA drug approvals

FDA approval · Drugs@FDA

STALEVO 75carbidopa, entacapone, levodopa

NDA021485 ·

FDA approved the original new drug application for STALEVO 75 on June 11, 2003, sponsored by ORION PHARMA. FDA’s record shows no approved efficacy supplement on the application since.

Application
NDA021485
Sponsor
ORION PHARMA
Original approval
Review
standard review
Submission class
Type 4 - New Combination
Active ingredient
carbidopa, entacapone, levodopa

Products under this application

Ingredient and strengthFormRouteMarketing status
carbidopa 18.75MG; entacapone 200MG; levodopa 75MGTABLETORALPrescription
carbidopa 37.5MG; entacapone 200MG; levodopa 150MGTABLETORALPrescription
carbidopa 12.5MG; entacapone 200MG; levodopa 50MGTABLETORALPrescription
carbidopa 31.25MG; entacapone 200MG; levodopa 125MGTABLETORALPrescription
carbidopa 50MG; entacapone 200MG; levodopa 200MGTABLETORALPrescription
carbidopa 25MG; entacapone 200MG; levodopa 100MGTABLETORALPrescription

Approved efficacy supplements

An efficacy supplement is how a sponsor asks FDA to approve a change that needs clinical evidence — most often a new indication. FDA’s record gives each one a submission number, a date and a review priority. It does not say what any supplement approved, so neither does this page. The approval letter and label for each are on accessdata.fda.gov under the application number.

FDA’s record shows no approved efficacy supplement on this application.

FDA records other approved supplements on this application, by the class code it assigns them: Labeling 9 · Manufacturing (CMC) 8 · Unclassified 1. Those are changes to the label or to how the drug is made rather than new clinical evidence, so they are counted here and not listed.

Source: FDA’s Drugs@FDA application file, via openFDA (export 2026-09-03). Every field on this page comes from that record.

Other approvals to ORION PHARMA

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