FdaApplication
ANDA 086386
Identifiers
- fda_app_no: ANDA086386
Properties
| Property | Value |
|---|---|
| applicant_name | WATSON LABORATORIES INC |
| application_type | ANDA |
| approval_date | 1983-06-17 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NANDROLONE PHENPROPIONATE | NANDROLONE PHENPROPIONATE | 25MG/ML | INJECTABLE;INJECTION |
1 product