Drug application
OXYBUTYNIN (OXYBUTYNIN)
Drugs@FDA ANDA 090526 · BARR LABS DIV TEVA
Key facts
| Drug name | OXYBUTYNIN |
|---|---|
| Active ingredients | OXYBUTYNIN |
| Application type | ANDA |
| Application number | 090526 |
| Company | BARR LABS DIV TEVA |
| Dosage forms | FILM, EXTENDED RELEASE, TRANSDERMAL |
| Strength | 3.9MG/24HR |
| Marketing status | Discontinued |
| Reference listed drug | No |
| Latest submission status date | Mar 4, 2014 |
At a glance
- 1–9 Submissions
- 1–9 Supplements
- None Label versions
- 1–9 Products
- None Therapeutic equivalents
- Yes FDA letters on file
- No FDA reviews on file
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.
Source: U.S. Food and Drug Administration (FDA), Drugs@FDA · Source date: