FdaApplication
ANDA 207891
Identifiers
- fda_app_no: ANDA207891
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMACEUTICAL INDUSTRIES LTD |
| application_type | ANDA |
| approval_date | 2018-10-12 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| OMEPRAZOLE | OMEPRAZOLE | 20MG | TABLET, DELAYED RELEASE;ORAL |
1 product