FdaApplication
ANDA 215880
Identifiers
- fda_app_no: ANDA215880
Properties
| Property | Value |
|---|---|
| applicant_name | MANKIND PHARMA LTD |
| application_type | ANDA |
| approval_date | 2022-07-26 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PANTOPRAZOLE SODIUM | PANTOPRAZOLE SODIUM | EQ 40MG BASE | TABLET, DELAYED RELEASE;ORAL |
| PANTOPRAZOLE SODIUM | PANTOPRAZOLE SODIUM | EQ 20MG BASE | TABLET, DELAYED RELEASE;ORAL |
2 products