FdaApplication
ANDA 214230
Identifiers
- fda_app_no: ANDA214230
Properties
| Property | Value |
|---|---|
| applicant_name | MANKIND PHARMA LTD |
| application_type | ANDA |
| approval_date | 2026-07-28 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| SUGAMMADEX SODIUM | SUGAMMADEX SODIUM | EQ 500MG BASE/5ML (EQ 100MG BASE/ML) | SOLUTION;INTRAVENOUS |
| SUGAMMADEX SODIUM | SUGAMMADEX SODIUM | EQ 200MG BASE/2ML (EQ 100MG BASE/ML) | SOLUTION;INTRAVENOUS |
2 products