FdaApplication
ANDA 075664
Identifiers
- fda_app_no: ANDA075664
Properties
| Property | Value |
|---|---|
| applicant_name | NEPHRON CORP |
| application_type | ANDA |
| approval_date | 2001-06-26 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ALBUTEROL SULFATE | ALBUTEROL SULFATE | EQ 0.5% BASE | SOLUTION;INHALATION |
1 product