FdaApplication
ANDA 218675
Identifiers
- fda_app_no: ANDA218675
Properties
| Property | Value |
|---|---|
| applicant_name | KNACK PHARMACEUTICALS INC |
| application_type | ANDA |
| approval_date | 2026-03-09 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DEXMEDETOMIDINE HYDROCHLORIDE | DEXMEDETOMIDINE HYDROCHLORIDE | EQ 200MCG BASE/2ML (EQ 100MCG BASE/ML) | INJECTABLE;INJECTION |
1 product