| NDC Code | 25021-162-68 |
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| Package Description | 10 VIAL in 1 CARTON (25021-162-68) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL |
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| Product NDC | 25021-162 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Oxacillin |
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| Non-Proprietary Name | Oxacillin Sodium |
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| Dosage Form | INJECTION, POWDER, FOR SOLUTION |
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| Usage | INTRAMUSCULAR; INTRAVENOUS |
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| Start Marketing Date | 20181015 |
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| End Marketing Date | 20250630 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA091246 |
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| Manufacturer | Sagent Pharmaceuticals |
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| Substance Name | OXACILLIN SODIUM |
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| Strength | 2 |
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| Strength Unit | g/1 |
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| Pharmacy Classes | Penicillin-class Antibacterial [EPC], Penicillins [CS] |
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