Drug application
ETHINYL ESTRADIOL; LEVONORGESTREL (ETHINYL ESTRADIOL, LEVONORGESTREL)
Drugs@FDA ANDA 206201 · MAYNE PHARMA INC
Key facts
| Drug name | ETHINYL ESTRADIOL; LEVONORGESTREL |
|---|---|
| Active ingredients | ETHINYL ESTRADIOL, LEVONORGESTREL |
| Application type | ANDA |
| Application number | 206201 |
| Company | MAYNE PHARMA INC |
| Dosage forms | TABLET, ORAL |
| Strength | 0.02MG,0.15MG;0.025MG,0.15MG;0.03MG,0.15MG;0.01MG,N/A |
| Marketing status | None (Tentative Approval) |
| Reference listed drug | No |
| Latest submission status date | Apr 28, 2017 |
At a glance
- 1–9 Submissions
- 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.