FdaApplication
NDA 020872
Identifiers
- fda_app_no: NDA020872
Properties
| Property | Value |
|---|---|
| applicant_name | CHATTEM INC DBA SANOFI CONSUMER HEALTHCARE |
| application_type | NDA |
| approval_date | 2011-01-24 |
Products (6)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ALLEGRA ALLERGY | FEXOFENADINE HYDROCHLORIDE | 60MG | TABLET;ORAL |
| ALLEGRA ALLERGY | FEXOFENADINE HYDROCHLORIDE | 180MG | TABLET;ORAL |
| ALLEGRA HIVES | FEXOFENADINE HYDROCHLORIDE | 180MG | TABLET;ORAL |
| ALLEGRA HIVES | FEXOFENADINE HYDROCHLORIDE | 60MG | TABLET;ORAL |
| CHILDREN'S ALLEGRA ALLERGY | FEXOFENADINE HYDROCHLORIDE | 30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
| CHILDREN'S ALLEGRA HIVES | FEXOFENADINE HYDROCHLORIDE | 30MG | TABLET;ORAL |
6 products