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FDA ANDA · ANDA077120

CARBIDOPA AND LEVODOPA

Sponsor: APOTEX INC

APPLICATION
ANDA077120
TYPE
ANDA
ORIGINAL APPROVAL
2008-06-02
LATEST ACTION
2026-05-28
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued

Products

CARBIDOPA AND LEVODOPADiscontinued
CARBIDOPA 10MG, LEVODOPA 100MG · TABLET · ORAL
CARBIDOPA AND LEVODOPADiscontinued
CARBIDOPA 25MG, LEVODOPA 100MG · TABLET · ORAL
CARBIDOPA AND LEVODOPADiscontinued
CARBIDOPA 25MG, LEVODOPA 250MG · TABLET · ORAL

Approval history

2026-05-28Labeling · Supplement 9 · standardAP
2021-02-04Labeling · Supplement 7 · standardAP
2016-01-04Labeling · Supplement 4 · standardAP
2010-12-29Labeling · Supplement 3AP
2008-06-02OriginalAP
VIEW ON DRUGS@FDA ↗

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Source: FDA Drugs@FDA. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data, not medical, legal, or regulatory advice.

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