ESOMEPRAZOLE SODIUM (ESOMEPRAZOLE SODIUM) — FDA Approval ANDA200882 (SUN PHARM)
ESOMEPRAZOLE SODIUM (ESOMEPRAZOLE SODIUM) — FDA Approval ANDA200882 (SUN PHARM) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: ESOMEPRAZOLE SODIUM; Active ingredients: ESOMEPRAZOLE SODIUM; Application number: ANDA200882.
| Brand name | ESOMEPRAZOLE SODIUM |
|---|---|
| Active ingredients | ESOMEPRAZOLE SODIUM |
| Application number | ANDA200882 |
| Sponsor | SUN PHARM |
| Dosage form | INJECTABLE |
| Route | INTRAVENOUS |
| Marketing status | Discontinued |
| Products in application | 2 |
| First approval date | 20130318 |
| Source | openFDA Drugs@FDA |
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