FdaApplication
ANDA 076355
Identifiers
- fda_app_no: ANDA076355
Properties
| Property | Value |
|---|---|
| applicant_name | NEPHRON PHARMACEUTICALS CORP |
| application_type | ANDA |
| approval_date | 2004-06-28 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ALBUTEROL SULFATE | ALBUTEROL SULFATE | EQ 0.042% BASE | SOLUTION;INHALATION |
| ALBUTEROL SULFATE | ALBUTEROL SULFATE | EQ 0.021% BASE | SOLUTION;INHALATION |
2 products