DIUCARDIN (HYDROFLUMETHIAZIDE) — FDA Approval ANDA083383 (WYETH AYERST)
DIUCARDIN (HYDROFLUMETHIAZIDE) — FDA Approval ANDA083383 (WYETH AYERST) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: DIUCARDIN; Active ingredients: HYDROFLUMETHIAZIDE; Application number: ANDA083383.
| Brand name | DIUCARDIN |
|---|---|
| Active ingredients | HYDROFLUMETHIAZIDE |
| Application number | ANDA083383 |
| Sponsor | WYETH AYERST |
| Dosage form | TABLET |
| Route | ORAL |
| Marketing status | Discontinued |
| Products in application | 1 |
| First approval date | 19731220 |
| Source | openFDA Drugs@FDA |
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