| NDC Code | 70518-2301-0 |
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| Package Description | 10 VIAL, SINGLE-USE in 1 CARTON (70518-2301-0) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE (70518-2301-1) |
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| Product NDC | 70518-2301 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Ceftriaxone Sodium |
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| Non-Proprietary Name | Ceftriaxone 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 | 20190904 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA065169 |
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| Manufacturer | REMEDYREPACK INC. |
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| Substance Name | CEFTRIAXONE SODIUM |
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| Strength | 500 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Cephalosporin Antibacterial [EPC], Cephalosporins [CS] |
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