FdaApplication
ANDA 076870
Identifiers
- fda_app_no: ANDA076870
Properties
| Property | Value |
|---|---|
| applicant_name | HIKMA PHARMS |
| application_type | ANDA |
| approval_date | 2004-08-26 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ALLOPURINOL SODIUM | ALLOPURINOL SODIUM | EQ 500MG BASE/VIAL | INJECTABLE;INJECTION |
1 product