FdaApplication
NDA 018039
Identifiers
- fda_app_no: NDA018039
Properties
| Property | Value |
|---|---|
| applicant_name | ACTAVIS LABORATORIES UT INC |
| application_type | NDA |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| LOXITANE IM | LOXAPINE HYDROCHLORIDE | EQ 50MG BASE/ML | INJECTABLE;INJECTION |
1 product