Drug application
GEMFIBROZIL (GEMFIBROZIL)
Drugs@FDA ANDA 072929 · PUREPAC PHARM
Key facts
| Drug name | GEMFIBROZIL |
|---|---|
| Active ingredients | GEMFIBROZIL |
| Application type | ANDA |
| Application number | 072929 |
| Company | PUREPAC PHARM |
| Dosage forms | CAPSULE, ORAL |
| Strength | 300MG |
| Marketing status | Discontinued |
| Reference listed drug | No |
| Latest submission status date | Oct 4, 1991 |
At a glance
- 1–9 Submissions
- 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.