FdaApplication
ANDA 071007
Identifiers
- fda_app_no: ANDA071007
Properties
| Property | Value |
|---|---|
| applicant_name | USL PHARMA INC |
| application_type | ANDA |
| approval_date | 1988-03-25 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| MECLOFENAMATE SODIUM | MECLOFENAMATE SODIUM | EQ 50MG BASE | CAPSULE;ORAL |
1 product