LARODOPA (LEVODOPA) — FDA Approval NDA016912 (ROCHE)
LARODOPA (LEVODOPA) — FDA Approval NDA016912 (ROCHE) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: LARODOPA; Active ingredients: LEVODOPA; Application number: NDA016912.
| Brand name | LARODOPA |
|---|---|
| Active ingredients | LEVODOPA |
| Application number | NDA016912 |
| Sponsor | ROCHE |
| Dosage form | TABLET |
| Route | ORAL |
| Marketing status | Discontinued |
| Products in application | 6 |
| First approval date | 19700604 |
| Source | openFDA Drugs@FDA |
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