Drug application
CLOFIBRATE (CLOFIBRATE)
Drugs@FDA ANDA 070531 · USL PHARMA
Key facts
| Drug name | CLOFIBRATE |
|---|---|
| Active ingredients | CLOFIBRATE |
| Application type | ANDA |
| Application number | 070531 |
| Company | USL PHARMA |
| Dosage forms | CAPSULE, ORAL |
| Strength | 500MG |
| Marketing status | Discontinued |
| Reference listed drug | No |
| Latest submission status date | Jun 16, 1986 |
At a glance
- 1–9 Submissions
- 10–99 Supplements
- 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.