FdaApplication
ANDA 203729
Identifiers
- fda_app_no: ANDA203729
Properties
| Property | Value |
|---|---|
| applicant_name | AMNEAL PHARMACEUTICALS |
| application_type | ANDA |
| approval_date | 2015-07-15 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| QUININE SULFATE | QUININE SULFATE | 324MG | CAPSULE;ORAL |
1 product