| NDC Code | 23155-906-41 |
|---|
| Package Description | 10 VIAL in 1 CARTON (23155-906-41) / 4 mL in 1 VIAL |
|---|
| Product NDC | 23155-906 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Nafcillin |
|---|
| Non-Proprietary Name | Nafcillin Sodium |
|---|
| Dosage Form | INJECTION, POWDER, FOR SOLUTION |
|---|
| Usage | INTRAMUSCULAR; INTRAVENOUS |
|---|
| Start Marketing Date | 20250215 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA090560 |
|---|
| Manufacturer | Heritage Pharmaceuticals Inc. d/b/a/ Avet Pharmaceuticals Inc. |
|---|
| Substance Name | NAFCILLIN SODIUM |
|---|
| Strength | 1 |
|---|
| Strength Unit | g/4mL |
|---|
| Pharmacy Classes | Penicillin-class Antibacterial [EPC], Penicillins [CS] |
|---|