Drug application
ATAZANAVIR SULFATE;RITONAVIR;LAMIVUDINE;ZIDOVUDINE (ATAZANAVIR SULFATE, RITONAVIR, LAMIVUDINE and 1 more)
Drugs@FDA NDA 206041 · MYLAN LABS LTD
Key facts
| Drug name | ATAZANAVIR SULFATE;RITONAVIR;LAMIVUDINE;ZIDOVUDINE |
|---|---|
| Active ingredients | ATAZANAVIR SULFATE, RITONAVIR, LAMIVUDINE, ZIDOVUDINE |
| Application type | NDA |
| Application number | 206041 |
| Company | MYLAN LABS LTD |
| Dosage forms | TABLET, ORAL |
| Strength | 300MG;100MG;150MG;300MG |
| Marketing status | None (Tentative Approval) |
| Reference listed drug | No |
| Latest submission class | Type 4 - New Combination |
| Latest submission status date | Sep 4, 2014 |
At a glance
- 1–9 Submissions
- 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: