General MedicationsORALGeneric
LARODOPA
LEVODOPA
Standard Dose
100MG
Max Dose
Refer to approved labeling
Primary Use
Review priority: PRIORITY Marketing status: Discontinued
Summary
Approval overview LARODOPA is listed in Drugs@FDA under application 016912 (NDA).
Review priority: PRIORITY Marketing status: Discontinued Active ingredient LEVODOPA Form and strength TABLET;ORAL - 100MG Sponsor ROCHE Submission history Latest submission status date: 1998-08-19 00:00:00.
Structured Monograph
Clinical summary
Approval overview LARODOPA is listed in Drugs@FDA under application 016912 (NDA). Review priority: PRIORITY Marketing status: Discontinued Active ingredient LEVODOPA Form and strength TABLET;ORAL - 100MG Sponsor ROCHE Submission history Latest submission status date: 1998-08-19 00:00:00. Submission type: SUPPL.
Monitoring
- • Marketing status: Discontinued
- • Review priority: PRIORITY
Interaction Notes
- No interaction notes stored yet.