FdaApplication
NDA 012329
Identifiers
- fda_app_no: NDA012329
Properties
| Property | Value |
|---|---|
| applicant_name | NOVARTIS PHARMACEUTICALS CORP |
| application_type | NDA |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ISMELIN | GUANETHIDINE MONOSULFATE | EQ 25MG SULFATE | TABLET;ORAL |
| ISMELIN | GUANETHIDINE MONOSULFATE | EQ 10MG SULFATE | TABLET;ORAL |
2 products