QUINIDINE SULFATE (QUINIDINE SULFATE) — FDA Approval ANDA081031 (SUN PHARM INDUSTRIES)
QUINIDINE SULFATE (QUINIDINE SULFATE) — FDA Approval ANDA081031 (SUN PHARM INDUSTRIES) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: QUINIDINE SULFATE; Active ingredients: QUINIDINE SULFATE; Application number: ANDA081031.
| Brand name | QUINIDINE SULFATE |
|---|---|
| Active ingredients | QUINIDINE SULFATE |
| Application number | ANDA081031 |
| Sponsor | SUN PHARM INDUSTRIES |
| Dosage form | TABLET |
| Route | ORAL |
| Marketing status | Discontinued |
| Products in application | 1 |
| First approval date | 19890414 |
| Source | openFDA Drugs@FDA |
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