Drug application
DALFAMPRIDINE (DALFAMPRIDINE)
Drugs@FDA ANDA 206854 · TEVA PHARMS USA INC
Key facts
| Drug name | DALFAMPRIDINE |
|---|---|
| Active ingredients | DALFAMPRIDINE |
| Application type | ANDA |
| Application number | 206854 |
| Company | TEVA PHARMS USA INC |
| Dosage forms | TABLET, EXTENDED RELEASE, ORAL |
| Strength | 10MG |
| Marketing status | None (Tentative Approval) |
| Reference listed drug | No |
| Latest submission status date | Jul 19, 2016 |
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.