| NDC Code | 70594-082-02 |
|---|
| Package Description | 10 VIAL in 1 CARTON (70594-082-02) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (70594-082-01) |
|---|
| Product NDC | 70594-082 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Ampicillin And Sulbactam |
|---|
| Non-Proprietary Name | Ampicillin Sodium And Sulbactam Sodium |
|---|
| Dosage Form | INJECTION, POWDER, FOR SOLUTION |
|---|
| Usage | INTRAMUSCULAR; INTRAVENOUS |
|---|
| Start Marketing Date | 20210110 |
|---|
| End Marketing Date | 20251231 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA090579 |
|---|
| Manufacturer | Xellia Pharmaceuticals USA LLC |
|---|
| Substance Name | AMPICILLIN SODIUM; SULBACTAM SODIUM |
|---|
| Strength | 2; 1 |
|---|
| Strength Unit | g/1; g/1 |
|---|
| Pharmacy Classes | Penicillin-class Antibacterial [EPC], Penicillins [CS], beta Lactamase Inhibitor [EPC], beta Lactamase Inhibitors [MoA] |
|---|