FdaApplication
ANDA 206332
Identifiers
- fda_app_no: ANDA206332
Properties
| Property | Value |
|---|---|
| applicant_name | NEXUS PHARMACEUTICALS LLC |
| application_type | ANDA |
| approval_date | 2017-10-13 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PROCAINAMIDE HYDROCHLORIDE | PROCAINAMIDE HYDROCHLORIDE | 100MG/ML | INJECTABLE;INJECTION |
| PROCAINAMIDE HYDROCHLORIDE | PROCAINAMIDE HYDROCHLORIDE | 500MG/ML | INJECTABLE;INJECTION |
2 products