FdaApplication
ANDA 201311
Identifiers
- fda_app_no: ANDA201311
Properties
| Property | Value |
|---|---|
| applicant_name | P AND L DEVELOPMENT LLC |
| application_type | ANDA |
| approval_date | 2012-07-25 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| FEXOFENADINE HYDROCHLORIDE | FEXOFENADINE HYDROCHLORIDE | 30MG/5ML | SUSPENSION;ORAL |
1 product