Drug application
LUPRON (LEUPROLIDE ACETATE)
Drugs@FDA NDA 019010 · ABBVIE ENDOCRINE INC
Key facts
| Drug name | LUPRON |
|---|---|
| Active ingredients | LEUPROLIDE ACETATE |
| Application type | NDA |
| Application number | 019010 |
| Company | ABBVIE ENDOCRINE INC |
| Dosage forms | SOLUTION, SUBCUTANEOUS |
| Strength | 14MG/2.8ML (1MG/0.2ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** |
| Marketing status | Discontinued |
| Reference listed drug | Yes |
| Latest submission class | Type 1 - New Molecular Entity |
| Latest submission status date | Apr 9, 1985 |
At a glance
- 1–9 Submissions
- 10–99 Supplements
- 10–99 Label versions
- 1–9 Products
- None Therapeutic equivalents
- No 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: