FdaApplication
NDA 203340
Identifiers
- fda_app_no: NDA203340
Properties
| Property | Value |
|---|---|
| applicant_name | AZURITY PHARMACEUTICALS INC |
| application_type | NDA |
| approval_date | 2013-05-10 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NYMALIZE | NIMODIPINE | 6MG/ML | SOLUTION;ORAL |
| NYMALIZE | NIMODIPINE | 3MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | SOLUTION;ORAL |
2 products