FdaApplication
ANDA 212363
Identifiers
- fda_app_no: ANDA212363
Properties
| Property | Value |
|---|---|
| applicant_name | GLAND PHARMA LTD |
| application_type | ANDA |
| approval_date | 2022-01-26 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ALLOPURINOL SODIUM | ALLOPURINOL SODIUM | EQ 500MG BASE/VIAL | INJECTABLE;INJECTION |
1 product