FdaApplication
ANDA 088256
Identifiers
- fda_app_no: ANDA088256
Properties
| Property | Value |
|---|---|
| applicant_name | UDL LABORATORIES INC |
| application_type | ANDA |
| approval_date | 1983-06-13 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| MECLIZINE HYDROCHLORIDE | MECLIZINE HYDROCHLORIDE | 12.5MG | TABLET;ORAL |
1 product