| NDC Code | 52125-680-01 |
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| Package Description | 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE (52125-680-01) |
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| Product NDC | 52125-680 |
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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 | 20140722 |
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| End Marketing Date | 20170302 |
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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 | 1 |
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| Strength Unit | g/1 |
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| Pharmacy Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |
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