FdaApplication
NDA 013294
Identifiers
- fda_app_no: NDA013294
Properties
| Property | Value |
|---|---|
| applicant_name | HOFFMANN LA ROCHE INC |
| application_type | NDA |
| approval_date | 1987-09-10 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| AZO GANTANOL | PHENAZOPYRIDINE HYDROCHLORIDE; SULFAMETHOXAZOLE | 100MG;500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
1 product