FdaApplication
ANDA 075906
Identifiers
- fda_app_no: ANDA075906
Properties
| Property | Value |
|---|---|
| applicant_name | FRESENIUS KABI USA LLC |
| application_type | ANDA |
| approval_date | 2001-04-25 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PROGESTERONE | PROGESTERONE | 50MG/ML | INJECTABLE;INJECTION |
1 product