Drug application
MINOLIRA (MINOCYCLINE HYDROCHLORIDE)
Drugs@FDA NDA 209269 · EPI HLTH
Key facts
| Drug name | MINOLIRA |
|---|---|
| Active ingredients | MINOCYCLINE HYDROCHLORIDE |
| Application type | NDA |
| Application number | 209269 |
| Company | EPI HLTH |
| Dosage forms | TABLET, EXTENDED RELEASE, ORAL |
| Strength | EQ 105MG BASE |
| Marketing status | Discontinued |
| Reference listed drug | No |
| Latest submission class | Type 5 - New Formulation or New Manufacturer |
| Latest submission status date | May 8, 2017 |
At a glance
- 1–9 Submissions
- None Label versions
- 1–9 Products
- None 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: