Drug application
DONEPEZIL HYDROCHLORIDE (DONEPEZIL HYDROCHLORIDE)
Drugs@FDA ANDA 090175 · ZYDUS PHARMS USA INC
Key facts
| Drug name | DONEPEZIL HYDROCHLORIDE |
|---|---|
| Active ingredients | DONEPEZIL HYDROCHLORIDE |
| Application type | ANDA |
| Application number | 090175 |
| Company | ZYDUS PHARMS USA INC |
| Dosage forms | TABLET, ORALLY DISINTEGRATING, ORAL |
| Strength | 5MG |
| Marketing status | Discontinued |
| Reference listed drug | No |
| Latest submission status date | May 10, 2011 |
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.