FdaApplication
ANDA 207096
Identifiers
- fda_app_no: ANDA207096
Properties
| Property | Value |
|---|---|
| applicant_name | AILEX PHARMACEUTICALS LLC |
| application_type | ANDA |
| approval_date | 2016-02-24 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| SODIUM PHENYLACETATE AND SODIUM BENZOATE | SODIUM BENZOATE; SODIUM PHENYLACETATE | 10%;10% (5GM/50ML | SOLUTION;INTRAVENOUS |
1 product