FdaApplication
ANDA 219200
Identifiers
- fda_app_no: ANDA219200
Properties
| Property | Value |
|---|---|
| applicant_name | ALKEM LABS LTD |
| application_type | ANDA |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| LUMATEPERONE | LUMATEPERONE | 42MG | CAPSULE |
| LUMATEPERONE | LUMATEPERONE | 21MG | CAPSULE |
| LUMATEPERONE | LUMATEPERONE | 10.5MG | CAPSULE |
3 products