FdaApplication
ANDA 209264
Identifiers
- fda_app_no: ANDA209264
Properties
| Property | Value |
|---|---|
| applicant_name | AILEX PHARMACEUTICALS LLC |
| application_type | ANDA |
| approval_date | 2017-10-16 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| CROMOLYN SODIUM | CROMOLYN SODIUM | 100MG/5ML | CONCENTRATE;ORAL |
1 product