FdaApplication
ANDA 209784
Identifiers
- fda_app_no: ANDA209784
Properties
| Property | Value |
|---|---|
| applicant_name | SANDOZ INC |
| application_type | ANDA |
| approval_date | 2017-08-23 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| EPHEDRINE SULFATE | EPHEDRINE SULFATE | 50MG/ML (50MG/ML) | SOLUTION;INTRAVENOUS |
1 product