RANOLAZINE (RANOLAZINE) — FDA Approval ANDA211707 (SUN PHARM)
RANOLAZINE (RANOLAZINE) — FDA Approval ANDA211707 (SUN PHARM) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: RANOLAZINE; Active ingredients: RANOLAZINE; Application number: ANDA211707.
| Brand name | RANOLAZINE |
|---|---|
| Active ingredients | RANOLAZINE |
| Application number | ANDA211707 |
| Sponsor | SUN PHARM |
| Dosage form | TABLET, EXTENDED RELEASE |
| Route | ORAL |
| Marketing status | Discontinued |
| Products in application | 2 |
| First approval date | 20190528 |
| Source | openFDA Drugs@FDA |
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