FdaApplication
ANDA 203660
Identifiers
- fda_app_no: ANDA203660
Properties
| Property | Value |
|---|---|
| applicant_name | EPIC PHARMA LLC |
| application_type | ANDA |
| approval_date | 2016-11-08 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| AZELASTINE HYDROCHLORIDE | AZELASTINE HYDROCHLORIDE | 0.05% | SOLUTION/DROPS;OPHTHALMIC |
1 product