NAPROXEN SODIUM (NAPROXEN SODIUM) — FDA Approval ANDA091183 (SUN PHARM INDS LTD)
NAPROXEN SODIUM (NAPROXEN SODIUM) — FDA Approval ANDA091183 (SUN PHARM INDS LTD) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: NAPROXEN SODIUM; Active ingredients: NAPROXEN SODIUM; Application number: ANDA091183.
| Brand name | NAPROXEN SODIUM |
|---|---|
| Active ingredients | NAPROXEN SODIUM |
| Application number | ANDA091183 |
| Sponsor | SUN PHARM INDS LTD |
| Dosage form | TABLET |
| Route | ORAL |
| Marketing status | Discontinued |
| Products in application | 1 |
| First approval date | 20110520 |
| Source | openFDA Drugs@FDA |
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