FdaApplication
ANDA 078192
Identifiers
- fda_app_no: ANDA078192
Properties
| Property | Value |
|---|---|
| applicant_name | DR REDDYS LABORATORIES LTD |
| application_type | ANDA |
| approval_date | 2007-08-31 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| RANITIDINE HYDROCHLORIDE | RANITIDINE HYDROCHLORIDE | EQ 150MG BASE | TABLET;ORAL |
1 product