FdaApplication
ANDA 215860
Identifiers
- fda_app_no: ANDA215860
Properties
| Property | Value |
|---|---|
| applicant_name | MEITHEAL PHARMACEUTICALS INC |
| application_type | ANDA |
| approval_date | 2022-08-29 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PANTOPRAZOLE SODIUM | PANTOPRAZOLE SODIUM | EQ 40MG BASE/VIAL | INJECTABLE;INTRAVENOUS |
1 product