Drug application
MINOXIDIL (FOR MEN) (MINOXIDIL)
Drugs@FDA ANDA 208092 · P AND L
Key facts
| Drug name | MINOXIDIL (FOR MEN) |
|---|---|
| Active ingredients | MINOXIDIL |
| Application type | ANDA |
| Application number | 208092 |
| Company | P AND L |
| Dosage forms | AEROSOL, FOAM, TOPICAL |
| Strength | 5% |
| Marketing status | Over-the-counter |
| Reference listed drug | No |
| Latest submission status date | Jul 27, 2017 |
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.
Source: U.S. Food and Drug Administration (FDA), Drugs@FDA · Source date: