FdaApplication
ANDA 210799
Identifiers
- fda_app_no: ANDA210799
Properties
| Property | Value |
|---|---|
| applicant_name | NOVITIUM PHARMA LLC |
| application_type | ANDA |
| approval_date | 2020-07-08 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DIAZOXIDE | DIAZOXIDE | 50MG/ML | SUSPENSION;ORAL |
1 product