FdaApplication
ANDA 213514
Identifiers
- fda_app_no: ANDA213514
Properties
| Property | Value |
|---|---|
| applicant_name | GLAND PHARMA LTD |
| application_type | ANDA |
| approval_date | 2026-01-06 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| OLOPATADINE HYDROCHLORIDE | OLOPATADINE HYDROCHLORIDE | EQ 0.7% BASE | SOLUTION/DROPS;OPHTHALMIC |
1 product