FdaApplication
ANDA 206606
Identifiers
- fda_app_no: ANDA206606
Properties
| Property | Value |
|---|---|
| applicant_name | ZYDUS PHARMACEUTICALS USA INC |
| application_type | ANDA |
| approval_date | 2017-06-13 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ACYCLOVIR SODIUM | ACYCLOVIR SODIUM | EQ 500MG BASE/VIAL | INJECTABLE;INJECTION |
| ACYCLOVIR SODIUM | ACYCLOVIR SODIUM | EQ 1GM BASE/VIAL | INJECTABLE;INJECTION |
2 products