FdaApplication
NDA 019667
Identifiers
- fda_app_no: NDA019667
Properties
| Property | Value |
|---|---|
| applicant_name | NOVARTIS PHARMACEUTICALS CORP |
| application_type | NDA |
| approval_date | 1988-10-21 |
Products (5)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| SANDOSTATIN | OCTREOTIDE ACETATE | EQ 1MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INJECTION |
| SANDOSTATIN | OCTREOTIDE ACETATE | EQ 0.05MG BASE/ML | INJECTABLE;INJECTION |
| SANDOSTATIN | OCTREOTIDE ACETATE | EQ 0.5MG BASE/ML | INJECTABLE;INJECTION |
| SANDOSTATIN | OCTREOTIDE ACETATE | EQ 0.1MG BASE/ML | INJECTABLE;INJECTION |
| SANDOSTATIN | OCTREOTIDE ACETATE | EQ 0.2MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INJECTION |
5 products