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FDA ANDA · ANDA078690

CARBIDOPA AND LEVODOPA

Sponsor: SUN PHARM

APPLICATION
ANDA078690
TYPE
ANDA
ORIGINAL APPROVAL
2009-07-31
LATEST ACTION
2009-07-31
ROUTE
ORAL
DOSAGE FORM
TABLET, ORALLY DISINTEGRATING
MARKETING STATUS
Prescription

Products

CARBIDOPA AND LEVODOPAPrescription
CARBIDOPA 25MG, LEVODOPA 250MG · TABLET, ORALLY DISINTEGRATING · ORAL
CARBIDOPA AND LEVODOPAPrescription
CARBIDOPA 10MG, LEVODOPA 100MG · TABLET, ORALLY DISINTEGRATING · ORAL
CARBIDOPA AND LEVODOPAPrescription
CARBIDOPA 25MG, LEVODOPA 100MG · TABLET, ORALLY DISINTEGRATING · ORAL

Approval history

2009-07-31OriginalAP
VIEW ON DRUGS@FDA ↗

Related on SPEQ

Pharma industry →GMP discipline →FDA drug shortages →FDA enforcement & recalls →

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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