FdaApplication
ANDA 071081
Identifiers
- fda_app_no: ANDA071081
Properties
| Property | Value |
|---|---|
| applicant_name | MYLAN PHARMACEUTICALS INC |
| application_type | ANDA |
| approval_date | 1986-09-03 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| MECLOFENAMATE SODIUM | MECLOFENAMATE SODIUM | EQ 50MG BASE | CAPSULE;ORAL |
| MECLOFENAMATE SODIUM | MECLOFENAMATE SODIUM | EQ 100MG BASE | CAPSULE;ORAL |
2 products