FdaApplication
ANDA 210174
Identifiers
- fda_app_no: ANDA210174
Properties
| Property | Value |
|---|---|
| applicant_name | AMNEAL EU LTD |
| application_type | ANDA |
| approval_date | 2017-10-27 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ZOLEDRONIC ACID | ZOLEDRONIC ACID | EQ 4MG BASE/100ML | INJECTABLE;INTRAVENOUS |
1 product