FdaApplication
ANDA 072630
Identifiers
- fda_app_no: ANDA072630
Properties
| Property | Value |
|---|---|
| applicant_name | WATSON LABORATORIES INC |
| application_type | ANDA |
| approval_date | 1991-01-31 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ALBUTEROL SULFATE | ALBUTEROL SULFATE | EQ 4MG BASE | TABLET;ORAL |
1 product