FdaApplication
ANDA 091027
Identifiers
- fda_app_no: ANDA091027
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMACEUTICAL INDUSTRIES INC |
| application_type | ANDA |
| approval_date | 2010-06-24 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| LITHIUM CARBONATE | LITHIUM CARBONATE | 300MG | TABLET;ORAL |
1 product