FdaApplication
ANDA 207321
Identifiers
- fda_app_no: ANDA207321
Properties
| Property | Value |
|---|---|
| applicant_name | GLAND PHARMA LTD |
| application_type | ANDA |
| approval_date | 2016-11-28 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DEXRAZOXANE HYDROCHLORIDE | DEXRAZOXANE HYDROCHLORIDE | EQ 500MG BASE/VIAL | INJECTABLE;INJECTION |
| DEXRAZOXANE HYDROCHLORIDE | DEXRAZOXANE HYDROCHLORIDE | EQ 250MG BASE/VIAL | INJECTABLE;INJECTION |
2 products