FdaApplication
ANDA 215822
Identifiers
- fda_app_no: ANDA215822
Properties
| Property | Value |
|---|---|
| applicant_name | VKT PHARMA PRIVATE LTD |
| application_type | ANDA |
| approval_date | 2022-01-28 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| FAMOTIDINE | FAMOTIDINE | 10MG | TABLET;ORAL |
| FAMOTIDINE | FAMOTIDINE | 20MG | TABLET;ORAL |
2 products