FdaApplication
NDA 209090
Identifiers
- fda_app_no: NDA209090
Properties
| Property | Value |
|---|---|
| applicant_name | CHATTEM INC DBA SANOFI CONSUMER HEALTHCARE |
| application_type | NDA |
| approval_date | 2017-01-31 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| XYZAL ALLERGY 24HR | LEVOCETIRIZINE DIHYDROCHLORIDE | 2.5MG/5ML | SOLUTION;ORAL |
1 product