Drug application
DEGARELIX ACETATE (DEGARELIX ACETATE)
Drugs@FDA ANDA 215791 · CHIA TAI TIANQING PHARMACEUTICAL GROUP CO., LTD.
Key facts
| Drug name | DEGARELIX ACETATE |
|---|---|
| Active ingredients | DEGARELIX ACETATE |
| Application type | ANDA |
| Application number | 215791 |
| Company | CHIA TAI TIANQING PHARMACEUTICAL GROUP CO., LTD. |
| Dosage forms | NJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Strength | 80MG |
| Marketing status | None (Tentative Approval) |
| Reference listed drug | No |
| Latest submission status date | Aug 18, 2025 |
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.