FdaApplication
NDA 211340
Identifiers
- fda_app_no: NDA211340
Properties
| Property | Value |
|---|---|
| applicant_name | AZURITY PHARMACEUTICALS INC |
| application_type | NDA |
| approval_date | 2019-07-08 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| KATERZIA | AMLODIPINE BENZOATE | EQ 1MG BASE/ML | SUSPENSION;ORAL |
1 product