FdaApplication
ANDA 076887
Identifiers
- fda_app_no: ANDA076887
Properties
| Property | Value |
|---|---|
| applicant_name | FRESENIUS KABI USA LLC |
| application_type | ANDA |
| approval_date | 2004-05-26 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| TERBUTALINE SULFATE | TERBUTALINE SULFATE | 1MG/ML | INJECTABLE;INJECTION |
1 product