FdaApplication
NDA 203195
Identifiers
- fda_app_no: NDA203195
Properties
| Property | Value |
|---|---|
| applicant_name | LUPIN LTD |
| application_type | NDA |
| approval_date | 2012-06-01 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| SUPRAX | CEFIXIME | 400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | CAPSULE;ORAL |
1 product