Drug application
QUARTETTE (ETHINYL ESTRADIOL, LEVONORGESTREL)
Drugs@FDA NDA 204061 · TEVA BRANDED PHARM
Key facts
| Drug name | QUARTETTE |
|---|---|
| Active ingredients | ETHINYL ESTRADIOL, LEVONORGESTREL |
| Application type | NDA |
| Application number | 204061 |
| Company | TEVA BRANDED PHARM |
| Dosage forms | TABLET, ORAL |
| Strength | 0.02MG,0.15MG;0.025MG,0.15MG;0.03MG,0.15MG;0.01MG,N/A |
| Marketing status | Prescription |
| TE codes | AB |
| Reference listed drug | Yes |
| Latest submission class | Type 5 - New Formulation or New Manufacturer |
| Latest submission status date | Mar 28, 2013 |
At a glance
- 1–9 Submissions
- 1–9 Supplements
- 1–9 Label versions
- 1–9 Products
- 1–9 Therapeutic equivalents
- Yes FDA letters on file
- Yes 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: