FdaApplication
ANDA 214201
Identifiers
- fda_app_no: ANDA214201
Properties
| Property | Value |
|---|---|
| applicant_name | ADAPTIS PHARMA PRIVATE LTD |
| application_type | ANDA |
| approval_date | 2022-06-27 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DIATRIZOATE MEGLUMINE AND DIATRIZOATE SODIUM | DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM | 66%;10% | SOLUTION;ORAL, RECTAL |
1 product