Drug application
METHYLNALTREXONE BROMIDE (METHYLNALTREXONE BROMIDE)
Drugs@FDA ANDA 208112 · ACTAVIS LLC
Key facts
| Drug name | METHYLNALTREXONE BROMIDE |
|---|---|
| Active ingredients | METHYLNALTREXONE BROMIDE |
| Application type | ANDA |
| Application number | 208112 |
| Company | ACTAVIS LLC |
| Dosage forms | SOLUTION, SUBCUTANEOUS |
| Strength | 8MG/0.4ML (8MG/0.4ML) |
| Marketing status | Discontinued |
| TE codes | AP |
| Reference listed drug | No |
| Latest submission status date | Aug 26, 2024 |
At a glance
- 1–9 Submissions
- None Label versions
- 1–9 Products
- 1–9 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.