CUPRIC SULFATE (CUPRIC SULFATE) — FDA Approval NDA019350 (ABRAXIS PHARM)
CUPRIC SULFATE (CUPRIC SULFATE) — FDA Approval NDA019350 (ABRAXIS PHARM) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: CUPRIC SULFATE; Active ingredients: CUPRIC SULFATE; Application number: NDA019350.
| Brand name | CUPRIC SULFATE |
|---|---|
| Active ingredients | CUPRIC SULFATE |
| Application number | NDA019350 |
| Sponsor | ABRAXIS PHARM |
| Dosage form | INJECTABLE |
| Route | INJECTION |
| Marketing status | Discontinued |
| Products in application | 1 |
| First approval date | 19870505 |
| Source | openFDA Drugs@FDA |
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