Drug application
BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE (BENAZEPRIL HYDROCHLORIDE, HYDROCHLOROTHIAZIDE)
Drugs@FDA ANDA 077483 · SUN PHARM INDS LTD
Key facts
| Drug name | BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE |
|---|---|
| Active ingredients | BENAZEPRIL HYDROCHLORIDE, HYDROCHLOROTHIAZIDE |
| Application type | ANDA |
| Application number | 077483 |
| Company | SUN PHARM INDS LTD |
| Dosage forms | TABLET, ORAL |
| Strength | 5MG;6.25MG |
| Marketing status | Discontinued |
| Reference listed drug | No |
| Latest submission status date | Sep 8, 2005 |
At a glance
- 1–9 Submissions
- 1–9 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.