FdaApplication
ANDA 216859
Identifiers
- fda_app_no: ANDA216859
Properties
| Property | Value |
|---|---|
| applicant_name | MANKIND PHARMA LTD |
| application_type | ANDA |
| approval_date | 2022-09-29 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PHENYLEPHRINE HYDROCHLORIDE | PHENYLEPHRINE HYDROCHLORIDE | 2.5% | SOLUTION/DROPS;OPHTHALMIC |
1 product