FdaApplication
NDA 203922
Identifiers
- fda_app_no: NDA203922
Properties
| Property | Value |
|---|---|
| applicant_name | HOPE PHARMACEUTICALS |
| application_type | NDA |
| approval_date | 2012-02-14 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| SODIUM NITRITE | SODIUM NITRITE | 300MG/10ML (30MG/ML) | SOLUTION;INTRAVENOUS |
1 product