CLOFIBRATE (CLOFIBRATE) — FDA Approval ANDA070531 (USL PHARMA)
CLOFIBRATE (CLOFIBRATE) — FDA Approval ANDA070531 (USL PHARMA) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: CLOFIBRATE; Active ingredients: CLOFIBRATE; Application number: ANDA070531.
| Brand name | CLOFIBRATE |
|---|---|
| Active ingredients | CLOFIBRATE |
| Application number | ANDA070531 |
| Sponsor | USL PHARMA |
| Dosage form | CAPSULE |
| Route | ORAL |
| Marketing status | Discontinued |
| Products in application | 1 |
| First approval date | 19860616 |
| Source | openFDA Drugs@FDA |
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