FdaApplication
ANDA 211289
Identifiers
- fda_app_no: ANDA211289
Properties
| Property | Value |
|---|---|
| applicant_name | VKT PHARMA PRIVATE LTD |
| application_type | ANDA |
| approval_date | 2019-01-31 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| RANITIDINE HYDROCHLORIDE | RANITIDINE HYDROCHLORIDE | EQ 300MG BASE | TABLET;ORAL |
| RANITIDINE HYDROCHLORIDE | RANITIDINE HYDROCHLORIDE | EQ 150MG BASE | TABLET;ORAL |
2 products