FdaApplication
ANDA 076835
Identifiers
- fda_app_no: ANDA076835
Properties
| Property | Value |
|---|---|
| applicant_name | EPIC PHARMA LLC |
| application_type | ANDA |
| approval_date | 2005-11-30 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| FLAVOXATE HYDROCHLORIDE | FLAVOXATE HYDROCHLORIDE | 100MG | TABLET;ORAL |
1 product