FdaApplication
ANDA 207350
Identifiers
- fda_app_no: ANDA207350
Properties
| Property | Value |
|---|---|
| applicant_name | HQ SPECIALTY PHARMA CORP |
| application_type | ANDA |
| approval_date | 2017-12-06 |
Products (5)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| MAGNESIUM SULFATE IN PLASTIC CONTAINER | MAGNESIUM SULFATE | 2GM/50ML (40MG/ML) | INJECTABLE;INJECTION |
| MAGNESIUM SULFATE IN PLASTIC CONTAINER | MAGNESIUM SULFATE | 4GM/100ML (40MG/ML) | INJECTABLE;INJECTION |
| MAGNESIUM SULFATE IN PLASTIC CONTAINER | MAGNESIUM SULFATE | 20GM/500ML (40MG/ML) | INJECTABLE;INJECTION |
| MAGNESIUM SULFATE IN PLASTIC CONTAINER | MAGNESIUM SULFATE | 40GM/1000ML (40MG/ML) | INJECTABLE;INJECTION |
| MAGNESIUM SULFATE IN PLASTIC CONTAINER | MAGNESIUM SULFATE | 4GM/50ML (80MG/ML) | INJECTABLE;INJECTION |
5 products