FdaApplication
ANDA 215035
Identifiers
- fda_app_no: ANDA215035
Properties
| Property | Value |
|---|---|
| applicant_name | AMNEAL PHARMACEUTICALS LLC |
| application_type | ANDA |
| approval_date | 2023-06-13 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| AMLODIPINE BENZOATE | AMLODIPINE BENZOATE | EQ 1MG BASE/ML | SUSPENSION;ORAL |
1 product