FdaApplication
ANDA 077476
Identifiers
- fda_app_no: ANDA077476
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMA CANADA INC |
| application_type | ANDA |
| approval_date | 2011-06-13 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| RANITIDINE HYDROCHLORIDE | RANITIDINE HYDROCHLORIDE | EQ 15MG BASE/ML | SYRUP;ORAL |
1 product