ULTRACEF (CEFADROXIL/CEFADROXIL HEMIHYDRATE) — FDA Approval ANDA062408 (BRISTOL)
ULTRACEF (CEFADROXIL/CEFADROXIL HEMIHYDRATE) — FDA Approval ANDA062408 (BRISTOL) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: ULTRACEF; Active ingredients: CEFADROXIL/CEFADROXIL HEMIHYDRATE; Application number: ANDA062408.
| Brand name | ULTRACEF |
|---|---|
| Active ingredients | CEFADROXIL/CEFADROXIL HEMIHYDRATE |
| Application number | ANDA062408 |
| Sponsor | BRISTOL |
| Dosage form | TABLET |
| Route | ORAL |
| Marketing status | Discontinued |
| Products in application | 1 |
| Source | openFDA Drugs@FDA |
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