FdaApplication
NDA 013132
Identifiers
- fda_app_no: NDA013132
Properties
| Property | Value |
|---|---|
| applicant_name | WOODWARD SPECIALTY LLC |
| application_type | NDA |
| approval_date | 1986-06-12 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DECA-DURABOLIN | NANDROLONE DECANOATE | 50MG/ML | INJECTABLE;INJECTION |
| DECA-DURABOLIN | NANDROLONE DECANOATE | 200MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INJECTION |
| DECA-DURABOLIN | NANDROLONE DECANOATE | 100MG/ML | INJECTABLE;INJECTION |
3 products