FdaApplication
NDA 020641
Identifiers
- fda_app_no: NDA020641
Properties
| Property | Value |
|---|---|
| applicant_name | BAYER HEALTHCARE LLC |
| application_type | NDA |
| approval_date | 2002-11-27 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| CLARITIN | LORATADINE | 1MG/ML | SYRUP;ORAL |
| CLARITIN HIVES RELIEF | LORATADINE | 1MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | SYRUP;ORAL |
2 products