FdaApplication
ANDA 076112
Identifiers
- fda_app_no: ANDA076112
Properties
| Property | Value |
|---|---|
| applicant_name | DR REDDYS LABORATORIES INC |
| application_type | ANDA |
| approval_date | 2001-10-31 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| IBUPROFEN | IBUPROFEN | 600MG | TABLET;ORAL |
| IBUPROFEN | IBUPROFEN | 400MG | TABLET;ORAL |
| IBUPROFEN | IBUPROFEN | 800MG | TABLET;ORAL |
3 products