Drug application
LEVALBUTEROL HYDROCHLORIDE (LEVALBUTEROL HYDROCHLORIDE)
Drugs@FDA ANDA 218770 · MANKIND PHARMA
Key facts
| Drug name | LEVALBUTEROL HYDROCHLORIDE |
|---|---|
| Active ingredients | LEVALBUTEROL HYDROCHLORIDE |
| Application type | ANDA |
| Application number | 218770 |
| Company | MANKIND PHARMA |
| Dosage forms | SOLUTION, INHALATION |
| Strength | EQ 0.0103% BASE |
| Marketing status | Discontinued |
| TE codes | AN |
| Reference listed drug | No |
| Latest submission status date | Oct 21, 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.