FdaApplication
ANDA 090125
Identifiers
- fda_app_no: ANDA090125
Properties
| Property | Value |
|---|---|
| applicant_name | NAVINTA LLC |
| application_type | ANDA |
| approval_date | 2009-11-17 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NICARDIPINE HYDROCHLORIDE | NICARDIPINE HYDROCHLORIDE | 25MG/10ML (2.5MG/ML) | INJECTABLE;INJECTION |
1 product