FdaApplication
NDA 205572
Identifiers
- fda_app_no: NDA205572
Properties
| Property | Value |
|---|---|
| applicant_name | FRESENIUS KABI USA LLC |
| application_type | NDA |
| approval_date | 2015-04-03 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| MOXIFLOXACIN HYDROCHLORIDE | MOXIFLOXACIN HYDROCHLORIDE | EQ 400MG BASE/250ML (EQ 1.6MG BASE/ML) | SOLUTION;INTRAVENOUS |
1 product