FdaApplication
ANDA 040718
Identifiers
- fda_app_no: ANDA040718
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMA CANADA INC |
| application_type | ANDA |
| approval_date | 2007-04-04 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PROMETHAZINE HYDROCHLORIDE | PROMETHAZINE HYDROCHLORIDE | 6.25MG/5ML | SYRUP;ORAL |
1 product