FdaApplication
NDA 006403
Identifiers
- fda_app_no: NDA006403
Properties
| Property | Value |
|---|---|
| applicant_name | NOVARTIS PHARMACEUTICALS CORP |
| application_type | NDA |
| approval_date | 1985-02-22 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PRISCOLINE | TOLAZOLINE HYDROCHLORIDE | 25MG/ML | INJECTABLE;INJECTION |
1 product