Drug application
OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE (HYDROCHLOROTHIAZIDE, OLMESARTAN MEDOXOMIL)
Drugs@FDA ANDA 078827 · NATCO PHARMA USA
Key facts
| Drug name | OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE |
|---|---|
| Active ingredients | HYDROCHLOROTHIAZIDE, OLMESARTAN MEDOXOMIL |
| Application type | ANDA |
| Application number | 078827 |
| Company | NATCO PHARMA USA |
| Dosage forms | TABLET, ORAL |
| Strength | 12.5MG;20MG |
| Marketing status | Discontinued |
| Reference listed drug | No |
| Latest submission status date | Oct 26, 2016 |
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: