Drug application
AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE (AMILORIDE HYDROCHLORIDE, HYDROCHLOROTHIAZIDE)
Drugs@FDA ANDA 073334 · WATSON LABS
Key facts
| Drug name | AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE |
|---|---|
| Active ingredients | AMILORIDE HYDROCHLORIDE, HYDROCHLOROTHIAZIDE |
| Application type | ANDA |
| Application number | 073334 |
| Company | WATSON LABS |
| Dosage forms | TABLET, ORAL |
| Strength | EQ 5MG ANHYDROUS;50MG |
| Marketing status | Discontinued |
| Reference listed drug | No |
| Latest submission status date | Jul 19, 1991 |
At a glance
- 1–9 Submissions
- 10–99 Supplements
- 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.