FdaApplication
ANDA 073121
Identifiers
- fda_app_no: ANDA073121
Properties
| Property | Value |
|---|---|
| applicant_name | UCB INC |
| application_type | ANDA |
| approval_date | 1992-09-29 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ALBUTEROL SULFATE | ALBUTEROL SULFATE | EQ 4MG BASE | TABLET;ORAL |
1 product