FdaApplication
ANDA 090018
Identifiers
- fda_app_no: ANDA090018
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMA GLOBAL FZE |
| application_type | ANDA |
| approval_date | 2013-03-04 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ZOLEDRONIC ACID | ZOLEDRONIC ACID | EQ 4MG BASE/VIAL | INJECTABLE;INTRAVENOUS |
1 product