FdaApplication
ANDA 075015
Identifiers
- fda_app_no: ANDA075015
Properties
| Property | Value |
|---|---|
| applicant_name | FRESENIUS KABI USA LLC |
| application_type | ANDA |
| approval_date | 1998-04-30 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ACYCLOVIR SODIUM | ACYCLOVIR SODIUM | EQ 500MG BASE/VIAL | INJECTABLE;INJECTION |
1 product