Drug application
ULTRACEF (CEFADROXIL/CEFADROXIL HEMIHYDRATE)
Drugs@FDA ANDA 062408 · BRISTOL
Key facts
| Drug name | ULTRACEF |
|---|---|
| Active ingredients | CEFADROXIL/CEFADROXIL HEMIHYDRATE |
| Application type | ANDA |
| Application number | 062408 |
| Company | BRISTOL |
| Dosage forms | TABLET, ORAL |
| Strength | EQ 1GM BASE |
| Marketing status | Discontinued |
| Reference listed drug | No |
At a glance
- None Label versions
- 1–9 Products
- None Therapeutic equivalents
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About Drugs@FDA applications
Drugs@FDA covers FDA-approved brand-name and generic drugs and therapeutic biologics, with their applications (NDA, ANDA or BLA), products, submissions and labels.