FdaApplication
ANDA 210070
Identifiers
- fda_app_no: ANDA210070
Properties
| Property | Value |
|---|---|
| applicant_name | APOTEX INC |
| application_type | ANDA |
| approval_date | 2019-02-11 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| OMEPRAZOLE | OMEPRAZOLE | 20MG | TABLET, DELAYED RELEASE;ORAL |
1 product