PANTOPRAZOLE SODIUM (PANTOPRAZOLE SODIUM) — FDA Approval ANDA077674 (SUN PHARM)
PANTOPRAZOLE SODIUM (PANTOPRAZOLE SODIUM) — FDA Approval ANDA077674 (SUN PHARM) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: PANTOPRAZOLE SODIUM; Active ingredients: PANTOPRAZOLE SODIUM; Application number: ANDA077674.
| Brand name | PANTOPRAZOLE SODIUM |
|---|---|
| Active ingredients | PANTOPRAZOLE SODIUM |
| Application number | ANDA077674 |
| Sponsor | SUN PHARM |
| Dosage form | INJECTABLE |
| Route | INTRAVENOUS |
| Marketing status | Discontinued |
| Products in application | 1 |
| First approval date | 20190819 |
| Source | openFDA Drugs@FDA |
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