FdaApplication
ANDA 211600
Identifiers
- fda_app_no: ANDA211600
Properties
| Property | Value |
|---|---|
| applicant_name | AMNEAL IRELAND LTD |
| application_type | ANDA |
| approval_date | 2025-12-01 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ALBUTEROL SULFATE | ALBUTEROL SULFATE | EQ 0.09MG BASE/INH | AEROSOL, METERED;INHALATION |
1 product