FdaApplication
ANDA 213552
Identifiers
- fda_app_no: ANDA213552
Properties
| Property | Value |
|---|---|
| applicant_name | NEXUS PHARMACEUTICALS LLC |
| application_type | ANDA |
| approval_date | 2020-10-27 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| SUCCINYLCHOLINE CHLORIDE | SUCCINYLCHOLINE CHLORIDE | 20MG/ML | INJECTABLE;INJECTION |
1 product