FdaApplication
ANDA 204222
Identifiers
- fda_app_no: ANDA204222
Properties
| Property | Value |
|---|---|
| applicant_name | APOTEX INC |
| application_type | ANDA |
| approval_date | 2015-10-16 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| IBANDRONATE SODIUM | IBANDRONATE SODIUM | EQ 3MG BASE/3ML | INJECTABLE;INTRAVENOUS |
1 product