FdaApplication
ANDA 213757
Identifiers
- fda_app_no: ANDA213757
Properties
| Property | Value |
|---|---|
| applicant_name | HIKMA PHARMS |
| application_type | ANDA |
| approval_date | 2020-08-19 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| OLOPATADINE HYDROCHLORIDE | OLOPATADINE HYDROCHLORIDE | 0.665MG/SPRAY | SPRAY, METERED;NASAL |
1 product