DURICEF (CEFADROXIL/CEFADROXIL HEMIHYDRATE) — FDA Approval NDA050512 (WARNER CHILCOTT)
DURICEF (CEFADROXIL/CEFADROXIL HEMIHYDRATE) — FDA Approval NDA050512 (WARNER CHILCOTT) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: DURICEF; Active ingredients: CEFADROXIL/CEFADROXIL HEMIHYDRATE; Application number: NDA050512.
| Brand name | DURICEF |
|---|---|
| Active ingredients | CEFADROXIL/CEFADROXIL HEMIHYDRATE |
| Application number | NDA050512 |
| Sponsor | WARNER CHILCOTT |
| Dosage form | CAPSULE |
| Route | ORAL |
| Marketing status | Discontinued |
| Products in application | 2 |
| First approval date | 19780217 |
| Source | openFDA Drugs@FDA |
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