Drug application
MIDODRINE HYDROCHLORIDE (MIDODRINE HYDROCHLORIDE)
Drugs@FDA ANDA 076577 · MYLAN PHARMS INC
Key facts
| Drug name | MIDODRINE HYDROCHLORIDE |
|---|---|
| Active ingredients | MIDODRINE HYDROCHLORIDE |
| Application type | ANDA |
| Application number | 076577 |
| Company | MYLAN PHARMS INC |
| Dosage forms | TABLET, ORAL |
| Strength | 2.5MG |
| Marketing status | Prescription |
| TE codes | AB |
| Reference listed drug | No |
| Latest submission status date | Sep 10, 2003 |
At a glance
- 1–9 Submissions
- 1–9 Supplements
- None Label versions
- 1–9 Products
- 10–99 Therapeutic equivalents
- No FDA letters on file
- Yes 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: