| NDC Code | 25021-162-24 |
|---|
| Package Description | 10 VIAL in 1 CARTON (25021-162-24) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL |
|---|
| Product NDC | 25021-162 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Oxacillin |
|---|
| Non-Proprietary Name | Oxacillin Sodium |
|---|
| Dosage Form | INJECTION, POWDER, FOR SOLUTION |
|---|
| Usage | INTRAMUSCULAR; INTRAVENOUS |
|---|
| Start Marketing Date | 20120601 |
|---|
| End Marketing Date | 20251130 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA091246 |
|---|
| Manufacturer | Sagent Pharmaceuticals |
|---|
| Substance Name | OXACILLIN SODIUM |
|---|
| Strength | 2 |
|---|
| Strength Unit | g/1 |
|---|
| Pharmacy Classes | Penicillin-class Antibacterial [EPC], Penicillins [CS] |
|---|