FdaApplication
NDA 019358
Identifiers
- fda_app_no: NDA019358
Properties
| Property | Value |
|---|---|
| applicant_name | HOFFMANN LA ROCHE INC |
| application_type | NDA |
| approval_date | 1990-08-31 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| AZO GANTRISIN | PHENAZOPYRIDINE HYDROCHLORIDE; SULFISOXAZOLE | 50MG;500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
1 product