FdaApplication
ANDA 210901
Identifiers
- fda_app_no: ANDA210901
Properties
| Property | Value |
|---|---|
| applicant_name | AMNEAL PHARMACEUTICALS LLC |
| application_type | ANDA |
| approval_date | 2020-01-28 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| OLOPATADINE HYDROCHLORIDE | OLOPATADINE HYDROCHLORIDE | 0.665MG/SPRAY | SPRAY, METERED;NASAL |
1 product