FdaApplication
ANDA 217271
Identifiers
- fda_app_no: ANDA217271
Properties
| Property | Value |
|---|---|
| applicant_name | MANKIND PHARMA LTD |
| application_type | ANDA |
| approval_date | 2023-11-01 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| MIDODRINE HYDROCHLORIDE | MIDODRINE HYDROCHLORIDE | 2.5MG | TABLET;ORAL |
| MIDODRINE HYDROCHLORIDE | MIDODRINE HYDROCHLORIDE | 10MG | TABLET;ORAL |
| MIDODRINE HYDROCHLORIDE | MIDODRINE HYDROCHLORIDE | 5MG | TABLET;ORAL |
3 products