FdaApplication
NDA 006002
Identifiers
- fda_app_no: NDA006002
Properties
| Property | Value |
|---|---|
| applicant_name | SANOFI AVENTIS US LLC |
| application_type | NDA |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ARALEN | CHLOROQUINE PHOSPHATE | 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
| ARALEN HYDROCHLORIDE | CHLOROQUINE HYDROCHLORIDE | EQ 40MG BASE/ML | INJECTABLE;INJECTION |
2 products