Drug application
OXTRIPHYLLINE (OXTRIPHYLLINE)
Drugs@FDA ANDA 087835 · WATSON LABS
Key facts
| Drug name | OXTRIPHYLLINE |
|---|---|
| Active ingredients | OXTRIPHYLLINE |
| Application type | ANDA |
| Application number | 087835 |
| Company | WATSON LABS |
| Dosage forms | TABLET, DELAYED RELEASE, ORAL |
| Strength | 200MG |
| 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.